Cancerous disease modifying antibodies

ABSTRACT

The present invention relates to a method for producing cancerous disease modifying antibodies using a novel paradigm of screening. By segregating the anti-cancer antibodies using cancer cell cytotoxicity as an end point, the process makes possible the production of anti-cancer antibodies for therapeutic and diagnostic purposes. The antibodies can be used in aid of staging and diagnosis of a cancer, and can be used to treat primary tumors and tumor metastases. The anti-cancer antibodies can be conjugated to toxins, enzymes, radioactive compounds, cytokines, interferons, target or reporter moieties and hematogenous cells.

REFERENCE TO RELATED APPLICATIONS

This application claims benefit of the filing date of ProvisionalApplication No. 60/776,548, filed on Feb. 24, 2006, the contents ofwhich are herein incorporated by reference.

FIELD OF THE INVENTION

This invention relates to the isolation and production of cancerousdisease modifying antibodies (CDMAB) and to the use of these CDMAB aloneor in combination with one or more CDMAB/chemotherapeutic agents intherapeutic and diagnostic processes. The invention further relates tobinding assays which utilize the CDMAB of the instant invention.

BACKGROUND OF THE INVENTION

Monoclonal Antibodies as Cancer Therapy: Each individual who presentswith cancer is unique and has a cancer that is as different from othercancers as that person's identity. Despite this, current therapy treatsall patients with the same type of cancer, at the same stage, in thesame way. At least 30 percent of these patients will fail the first linetherapy, thus leading to further rounds of treatment and the increasedprobability of treatment failure, metastases, and ultimately, death. Asuperior approach to treatment would be the customization of therapy forthe particular individual. The only current therapy which lends itselfto customization is surgery. Chemotherapy and radiation treatment cannotbe tailored to the patient, and surgery by itself, in most cases isinadequate for producing cures.

With the advent of monoclonal antibodies, the possibility of developingmethods for customized therapy became more realistic since each antibodycan be directed to a single epitope. Furthermore, it is possible toproduce a combination of antibodies that are directed to theconstellation of epitopes that uniquely define a particular individual'stumor.

Having recognized that a significant difference between cancerous andnormal cells is that cancerous cells contain antigens that are specificto transformed cells, the scientific community has long held thatmonoclonal antibodies can be designed to specifically target transformedcells by binding specifically to these cancer antigens; thus giving riseto the belief that monoclonal antibodies can serve as “Magic Bullets” toeliminate cancer cells. However, it is now widely recognized that nosingle monoclonal antibody can serve in all instances of cancer, andthat monoclonal antibodies can be deployed, as a class, as targetedcancer treatments. Monoclonal antibodies isolated in accordance with theteachings of the instantly disclosed invention have been shown to modifythe cancerous disease process in a manner which is beneficial to thepatient, for example by reducing the tumor burden, and will variously bereferred to herein as cancerous disease modifying antibodies (CDMAB) or“anti-cancer” antibodies.

At the present time, the cancer patient usually has few options oftreatment. The regimented approach to cancer therapy has producedimprovements in global survival and morbidity rates. However, to theparticular individual, these improved statistics do not necessarilycorrelate with an improvement in their personal situation.

Thus, if a methodology was put forth which enabled the practitioner totreat each tumor independently of other patients in the same cohort,this would permit the unique approach of tailoring therapy to just thatone person. Such a course of therapy would, ideally, increase the rateof cures, and produce better outcomes, thereby satisfying a long-feltneed.

Historically, the use of polyclonal antibodies has been used withlimited success in the treatment of human cancers. Lymphomas andleukemias have been treated with human plasma, but there were fewprolonged remission or responses. Furthermore, there was a lack ofreproducibility and there was no additional benefit compared tochemotherapy. Solid tumors such as breast cancers, melanomas and renalcell carcinomas have also been treated with human blood, chimpanzeeserum, human plasma and horse serum with correspondingly unpredictableand ineffective results.

There have been many clinical trials of monoclonal antibodies for solidtumors. In the 1980s there were at least four clinical trials for humanbreast cancer which produced only one responder from at least 47patients using antibodies against specific antigens or based on tissueselectivity. It was not until 1998 that there was a successful clinicaltrial using a humanized anti-Her2/neu antibody (Herceptin®) incombination with CISPLATIN. In this trial 37 patients were assessed forresponses of which about a quarter had a partial response rate and anadditional quarter had minor or stable disease progression. The mediantime to progression among the responders was 8.4 months with medianresponse duration of 5.3 months.

Herceptin® was approved in 1998 for first line use in combination withTaxol®. Clinical study results showed an increase in the median time todisease progression for those who received antibody therapy plus Taxol®(6.9 months) in comparison to the group that received Taxol® alone (3.0months). There was also a slight increase in median survival; 22 versus18 months for the Herceptin® plus Taxol® treatment arm versus the Taxol®treatment alone arm. In addition, there was an increase in the number ofboth complete (8 versus 2 percent) and partial responders (34 versus 15percent) in the antibody plus Taxol® combination group in comparison toTaxol® alone. However, treatment with Herceptin® and Taxol® led to ahigher incidence of cardiotoxicity in comparison to Taxol® treatmentalone (13 versus 1 percent respectively). Also, Herceptin® therapy wasonly effective for patients who over express (as determined throughimmunohistochemistry (IHC) analysis) the human epidermal growth factorreceptor 2 (Her2/neu), a receptor, which currently has no known functionor biologically important ligand; approximately 25 percent of patientswho have metastatic breast cancer. Therefore, there is still a largeunmet need for patients with breast cancer. Even those who can benefitfrom Herceptin® treatment would still require chemotherapy andconsequently would still have to deal with, at least to some degree, theside effects of this kind of treatment.

The clinical trials investigating colorectal cancer involve antibodiesagainst both glycoprotein and glycolipid targets. Antibodies such as17-1A, which has some specificity for adenocarcinomas, has undergonePhase 2 clinical trials in over 60 patients with only 1 patient having apartial response. In other trials, use of 17-1A produced only 1 completeresponse and 2 minor responses among 52 patients in protocols usingadditional cyclophosphamide. To date, Phase III clinical trials of 17-1Ahave not demonstrated improved efficacy as adjuvant therapy for stageIII colon cancer. The use of a humanized murine monoclonal antibodyinitially approved for imaging also did not produce tumor regression.

Only recently have there been any positive results from colorectalcancer clinical studies with the use of monoclonal antibodies. In 2004,ERBITUX® was approved for the second line treatment of patients withEGFR-expressing metastatic colorectal cancer who are refractory toirinotecan-based chemotherapy. Results from both a two-arm Phase IIclinical study and a single arm study showed that ERBITUX® incombination with irinotecan had a response rate of 23 and 15 percentrespectively with a median time to disease progression of 4.1 and 6.5months respectively. Results from the same two-arm Phase II clinicalstudy and another single arm study showed that treatment with ERBITUX®alone resulted in an 11 and 9 percent response rate respectively with amedian time to disease progression of 1.5 and 4.2 months respectively.

Consequently in both Switzerland and the United States, ERBITUX®treatment in combination with irinotecan, and in the United States,ERBITUX® treatment alone, has been approved as a second line treatmentof colon cancer patients who have failed first line irinotecan therapy.Therefore, like Herceptin®, treatment in Switzerland is only approved asa combination of monoclonal antibody and chemotherapy. In addition,treatment in both Switzerland and the US is only approved for patientsas a second line therapy. Also, in 2004, AVASTIN® was approved for usein combination with intravenous 5-fluorouracil-based chemotherapy as afirst line treatment of metastatic colorectal cancer. Phase III clinicalstudy results demonstrated a prolongation in the median survival ofpatients treated with AVASTIN® plus 5-fluorouracil compared to patientstreated with 5-fluourouracil alone (20 months versus 16 monthsrespectively). However, again like Herceptin® and ERBITUX®, treatment isonly approved as a combination of monoclonal antibody and chemotherapy.

There also continues to be poor results for lung, brain, ovarian,pancreatic, prostate, and stomach cancer. The most promising recentresults for non-small cell lung cancer came from a Phase II clinicaltrial where treatment involved a monoclonal antibody (SGN-15; dox-BR96,anti-Sialyl-LeX) conjugated to the cell-killing drug doxorubicin incombination with the chemotherapeutic agent TAXOTERE®. TAXOTERE® is theonly FDA approved chemotherapy for the second line treatment of lungcancer. Initial data indicate an improved overall survival compared toTAXOTERE® alone. Out of the 62 patients who were recruited for thestudy, two-thirds received SGN-15 in combination with TAXOTERE® whilethe remaining one-third received TAXOTERE® alone. For the patientsreceiving SGN-15 in combination with TAXOTERE®, median overall survivalwas 7.3 months in comparison to 5.9 months for patients receivingTAXOTERE® alone. Overall survival at 1 year and 18 months was 29 and 18percent respectively for patients receiving SNG-15 plus TAXOTERE®compared to 24 and 8 percent respectively for patients receivingTAXOTERE® alone. Further clinical trials are planned.

Preclinically, there has been some limited success in the use ofmonoclonal antibodies for melanoma. Very few of these antibodies havereached clinical trials and to date none have been approved ordemonstrated favorable results in Phase III clinical trials.

The discovery of new drugs to treat disease is hindered by the lack ofidentification of relevant targets among the products of 30,000 knowngenes that could contribute to disease pathogenesis. In oncologyresearch, potential drug targets are often selected simply due to thefact that they are over-expressed in tumor cells. Targets thusidentified are then screened for interaction with a multitude ofcompounds. In the case of potential antibody therapies, these candidatecompounds are usually derived from traditional methods of monoclonalantibody generation according to the fundamental principles laid down byKohler and Milstein (1975, Nature, 256, 495-497, Kohler and Milstein).Spleen cells are collected from mice immunized with antigen (e.g. wholecells, cell fractions, purified antigen) and fused with immortalizedhybridoma partners. The resulting hybridomas are screened and selectedfor secretion of antibodies which bind most avidly to the target. Manytherapeutic and diagnostic antibodies directed against cancer cells,including Herceptin® and RITUXIMAB, have been produced using thesemethods and selected on the basis of their affinity. The flaws in thisstrategy are two-fold. Firstly, the choice of appropriate targets fortherapeutic or diagnostic antibody binding is limited by the paucity ofknowledge surrounding tissue specific carcinogenic processes and theresulting simplistic methods, such as selection by overexpression, bywhich these targets are identified. Secondly, the assumption that thedrug molecule that binds to the receptor with the greatest affinityusually has the highest probability for initiating or inhibiting asignal may not always be the case.

Despite some progress with the treatment of breast and colon cancer, theidentification and development of efficacious antibody therapies, eitheras single agents or co-treatments, have been inadequate for all types ofcancer.

Prior Patents:

U.S. Pat. No. 5,750,102 discloses a process wherein cells from apatient's tumor are transfected with MHC genes which may be cloned fromcells or tissue from the patient. These transfected cells are then usedto vaccinate the patient.

U.S. Pat. No. 4,861,581 discloses a process comprising the steps ofobtaining monoclonal antibodies that are specific to an internalcellular component of neoplastic and normal cells of the mammal but notto external components, labeling the monoclonal antibody, contacting thelabeled antibody with tissue of a mammal that has received therapy tokill neoplastic cells, and determining the effectiveness of therapy bymeasuring the binding of the labeled antibody to the internal cellularcomponent of the degenerating neoplastic cells. In preparing antibodiesdirected to human intracellular antigens, the patentee recognizes thatmalignant cells represent a convenient source of such antigens.

U.S. Pat. No. 5,171,665 provides a novel antibody and method for itsproduction. Specifically, the patent teaches formation of a monoclonalantibody which has the property of binding strongly to a protein antigenassociated with human tumors, e.g. those of the colon and lung, whilebinding to normal cells to a much lesser degree.

U.S. Pat. No. 5,484,596 provides a method of cancer therapy comprisingsurgically removing tumor tissue from a human cancer patient, treatingthe tumor tissue to obtain tumor cells, irradiating the tumor cells tobe viable but non-tumorigenic, and using these cells to prepare avaccine for the patient capable of inhibiting recurrence of the primarytumor while simultaneously inhibiting metastases. The patent teaches thedevelopment of monoclonal antibodies which are reactive with surfaceantigens of tumor cells. As set forth at col. 4, lines 45 et seq., thepatentees utilize autochthonous tumor cells in the development ofmonoclonal antibodies expressing active specific immunotherapy in humanneoplasia.

U.S. Pat. No. 5,693,763 teaches a glycoprotein antigen characteristic ofhuman carcinomas and not dependent upon the epithelial tissue of origin.

U.S. Pat. No. 5,783,186 is drawn to Anti-Her2 antibodies which induceapoptosis in Her2 expressing cells, hybridoma cell lines producing theantibodies, methods of treating cancer using the antibodies andpharmaceutical compositions including said antibodies.

U.S. Pat. No. 5,849,876 describes new hybridoma cell lines for theproduction of monoclonal antibodies to mucin antigens purified fromtumor and non-tumor tissue sources.

U.S. Pat. No. 5,869,268 is drawn to a method for generating a humanlymphocyte producing an antibody specific to a desired antigen, a methodfor producing a monoclonal antibody, as well as monoclonal antibodiesproduced by the method. The patent is particularly drawn to theproduction of an anti-HD human monoclonal antibody useful for thediagnosis and treatment of cancers.

U.S. Pat. No. 5,869,045 relates to antibodies, antibody fragments,antibody conjugates and single-chain immunotoxins reactive with humancarcinoma cells. The mechanism by which these antibodies function istwo-fold, in that the molecules are reactive with cell membrane antigenspresent on the surface of human carcinomas, and further in that theantibodies have the ability to internalize within the carcinoma cells,subsequent to binding, making them especially useful for formingantibody-drug and antibody-toxin conjugates. In their unmodified formthe antibodies also manifest cytotoxic properties at specificconcentrations.

U.S. Pat. No. 5,780,033 discloses the use of autoantibodies for tumortherapy and prophylaxis. However, this antibody is an antinuclearautoantibody from an aged mammal. In this case, the autoantibody is saidto be one type of natural antibody found in the immune system. Becausethe autoantibody comes from “an aged mammal”, there is no requirementthat the autoantibody actually comes from the patient being treated. Inaddition the patent discloses natural and monoclonal antinuclearautoantibody from an aged mammal, and a hybridoma cell line producing amonoclonal antinuclear autoantibody.

SUMMARY OF THE INVENTION

This application utilizes methodology for producing patient specificanti-cancer antibodies taught in the U.S. Pat. No. 6,180,357 patent forisolating hybridoma cell lines which encode for cancerous diseasemodifying monoclonal antibodies. These antibodies can be madespecifically for one tumor and thus make possible the customization ofcancer therapy. Within the context of this application, anti-cancerantibodies having either cell-killing (cytotoxic) or cell-growthinhibiting (cytostatic) properties will hereafter be referred to ascytotoxic. These antibodies can be used in aid of staging and diagnosisof a cancer, and can be used to treat tumor metastases. These antibodiescan also be used for the prevention of cancer by way of prophylactictreatment. Unlike antibodies generated according to traditional drugdiscovery paradigms, antibodies generated in this way may targetmolecules and pathways not previously shown to be integral to the growthand/or survival of malignant tissue. Furthermore, the binding affinitiesof these antibodies are suited to requirements for initiation of thecytotoxic events that may not be amenable to stronger affinityinteractions. Also, it is within the purview of this invention toconjugate standard chemotherapeutic modalities, e.g. radionuclides, withthe CDMAB of the instant invention, thereby focusing the use of saidchemotherapeutics. The CDMAB can also be conjugated to toxins, cytotoxicmoieties, enzymes e.g. biotin conjugated enzymes, cytokines,interferons, target or reporter moieties or hematogenous cells, therebyforming an antibody conjugate. The CDMAB can be used alone or incombination with one or more CDMAB/chemotherapeutic agents.

The prospect of individualized anti-cancer treatment will bring about achange in the way a patient is managed. A likely clinical scenario isthat a tumor sample is obtained at the time of presentation, and banked.From this sample, the tumor can be typed from a panel of pre-existingcancerous disease modifying antibodies. The patient will beconventionally staged but the available antibodies can be of use infurther staging the patient. The patient can be treated immediately withthe existing antibodies, and a panel of antibodies specific to the tumorcan be produced either using the methods outlined herein or through theuse of phage display libraries in conjunction with the screening methodsherein disclosed. All the antibodies generated will be added to thelibrary of anti-cancer antibodies since there is a possibility thatother tumors can bear some of the same epitopes as the one that is beingtreated. The antibodies produced according to this method may be usefulto treat cancerous disease in any number of patients who have cancersthat bind to these antibodies.

In addition to anti-cancer antibodies, the patient can elect to receivethe currently recommended therapies as part of a multi-modal regimen oftreatment. The fact that the antibodies isolated via the presentmethodology are relatively non-toxic to non-cancerous cells allows forcombinations of antibodies at high doses to be used, either alone, or inconjunction with conventional therapy. The high therapeutic index willalso permit re-treatment on a short time scale that should decrease thelikelihood of emergence of treatment resistant cells.

If the patient is refractory to the initial course of therapy ormetastases develop, the process of generating specific antibodies to thetumor can be repeated for re-treatment. Furthermore, the anti-cancerantibodies can be conjugated to red blood cells obtained from thatpatient and re-infused for treatment of metastases. There have been feweffective treatments for metastatic cancer and metastases usuallyportend a poor outcome resulting in death. However, metastatic cancersare usually well vascularized and the delivery of anti-cancer antibodiesby red blood cells can have the effect of concentrating the antibodiesat the site of the tumor. Even prior to metastases, most cancer cellsare dependent on the host's blood supply for their survival and ananti-cancer antibody conjugated to red blood cells can be effectiveagainst in situ tumors as well. Alternatively, the antibodies may beconjugated to other hematogenous cells, e.g. lymphocytes, macrophages,monocytes, natural killer cells, etc.

There are five classes of antibodies and each is associated with afunction that is conferred by its heavy chain. It is generally thoughtthat cancer cell killing by naked antibodies are mediated either throughantibody dependent cellular cytotoxicity (ADCC) or complement dependentcytotoxicity (CDC). For example murine IgM and IgG2a antibodies canactivate human complement by binding the C-1 component of the complementsystem thereby activating the classical pathway of complement activationwhich can lead to tumor lysis. For human antibodies the most effectivecomplement activating antibodies are generally IgM and IgG1. Murineantibodies of the IgG2a and IgG3 isotype are effective at recruitingcytotoxic cells that have Fc receptors which will lead to cell killingby monocytes, macrophages, granulocytes and certain lymphocytes. Humanantibodies of both the IgG1 and IgG3 isotype mediate ADCC.

The cytotoxicity mediated through the Fc region requires the presence ofeffector cells, their corresponding receptors, or proteins e.g. NKcells, T cells and complement. In the absence of these effectormechanisms, the Fc portion of an antibody is inert. The Fc portion of anantibody may confer properties that affect the pharmacokinetics of anantibody in vivo, but in vitro this is not operative.

The cytotoxicity assays under which we test the antibodies do not haveany of the effector mechanisms present, and are carried out in vitro.These assays do not have effector cells (NK, Macrophages, or T-cells) orcomplement present. Since these assays are completely defined by what isadded together, each component can be characterized. The assays usedherein contain only target cells, media and sera. The target cells donot have effector functions since they are cancer cells or fibroblasts.Without exogenous cells which have effector function properties there isno cellular elements that have this function. The media does not containcomplement or any cells. The sera used to support the growth of thetarget cells do not have complement activity as disclosed by thevendors. Furthermore, in our own labs we have verified the absence ofcomplement activity in the sera used. Therefore, our work evidences thefact that the effects of the antibodies are due entirely to the effectsof the antigen binding which is mediated through the Fab. Effectively,the target cells are seeing and interacting with only the Fab, sincethey do not have receptors for the Fc. Although the hybridoma issecreting complete immunoglobulin which was tested with the targetcells, the only part of the immunoglobulin that interacts with the cellsare the Fab, which act as antigen binding fragments.

With respect to the instantly claimed antibodies and antigen bindingfragments, the application, as filed, has demonstrated cellularcytotoxicity as evidenced by the data in FIG. 1. As pointed out above,and as herein confirmed via objective evidence, this effect was entirelydue to binding by the Fab to the tumor cells.

Ample evidence exists in the art of antibodies mediating cytotoxicitydue to direct binding of the antibody to the target antigen independentof effector mechanisms recruited by the Fc. The best evidence for thisis in vitro experiments which do not have supplemental cells, orcomplement (to formally exclude those mechanisms). These types ofexperiments have been carried out with complete immunoglobulin, or withantigen binding fragments such as F(ab)′2 fragments. In these types ofexperiments, antibodies or antigen binding fragments can directly induceapoptosis of target cells such as in the case of anti-Her2 and anti-EGFRantibodies, both of which have been approved by the US FDA for marketingin cancer therapy.

Another possible mechanism of antibody mediated cancer killing may bethrough the use of antibodies that function to catalyze the hydrolysisof various chemical bonds in the cell membrane and its associatedglycoproteins or glycolipids, so-called catalytic antibodies.

There are three additional mechanisms of antibody-mediated cancer cellkilling. The first is the use of antibodies as a vaccine to induce thebody to produce an immune response against the putative antigen thatresides on the cancer cell. The second is the use of antibodies totarget growth receptors and interfere with their function or to downregulate that receptor so that its function is effectively lost. Thethird is the effect of such antibodies on direct ligation of cellsurface moieties that may lead to direct cell death, such as ligation ofdeath receptors such as TRAIL R1 or TRAIL R2, or integrin molecules suchas alpha V beta 3 and the like.

The clinical utility of a cancer drug is based on the benefit of thedrug under an acceptable risk profile to the patient. In cancer therapysurvival has generally been the most sought after benefit, however thereare a number of other well-recognized benefits in addition to prolonginglife. These other benefits, where treatment does not adversely affectsurvival, include symptom palliation, protection against adverse events,prolongation in time to recurrence or disease-free survival, andprolongation in time to progression. These criteria are generallyaccepted and regulatory bodies such as the U.S. Food and DrugAdministration (F.D.A.) approve drugs that produce these benefits(Hirschfeld et al. Critical Reviews in Oncology/Hematolgy 42:137-1432002). In addition to these criteria it is well recognized that thereare other endpoints that may presage these types of benefits. In part,the accelerated approval process granted by the U.S. F.D.A. acknowledgesthat there are surrogates that will likely predict patient benefit. Asof year-end 2003, there have been sixteen drugs approved under thisprocess, and of these, four have gone on to full approval, i.e.,follow-up studies have demonstrated direct patient benefit as predictedby surrogate endpoints. One important endpoint for determining drugeffects in solid tumors is the assessment of tumor burden by measuringresponse to treatment (Therasse et al. Journal of the National CancerInstitute 92(3):205-216 2000). The clinical criteria (RECIST criteria)for such evaluation have been promulgated by Response EvaluationCriteria in Solid Tumors Working Group, a group of international expertsin cancer. Drugs with a demonstrated effect on tumor burden, as shown byobjective responses according to RECIST criteria, in comparison to theappropriate control group tend to, ultimately, produce direct patientbenefit. In the pre-clinical setting tumor burden is generally morestraightforward to assess and document. In that pre-clinical studies canbe translated to the clinical setting, drugs that produce prolongedsurvival in pre-clinical models have the greatest anticipated clinicalutility. Analogous to producing positive responses to clinicaltreatment, drugs that reduce tumor burden in the pre-clinical settingmay also have significant direct impact on the disease. Althoughprolongation of survival is the most sought after clinical outcome fromcancer drug treatment, there are other benefits that have clinicalutility and it is clear that tumor burden reduction, which may correlateto a delay in disease progression, extended survival or both, can alsolead to direct benefits and have clinical impact (Eckhardt et al.Developmental Therapeutics: Successes and Failures of Clinical TrialDesigns of Targeted Compounds; ASCO Educational Book, 39^(th) AnnualMeeting, 2003, pages 209-219).

The present invention describes the development and use of AR53A10.11identified by, its effect, in a cytotoxic assay and in a non-establishedanimal model. This invention describes reagents that bind specificallyto an epitope or epitopes present on the target molecule, and that alsohave in vitro cytotoxic properties, as a naked antibody, againstmalignant tumor cells but not normal cells, and which also directlymediate, as a naked antibody, inhibition of tumor growth. A furtheradvance is that inclusion of this antibody in a library of anti-cancerantibodies will enhance the possibility of targeting tumors expressingdifferent antigen markers by determination of the appropriatecombination of different anti-cancer antibodies, to find the mosteffective in targeting and inhibiting growth and development of thetumors. It also represents an advance in cancer therapy since it has thepotential to display similar anti-cancer properties in human patients. Afurther advance is that inclusion of these antibodies in a library ofanti-cancer antibodies will enhance the possibility of targeting tumorsexpressing different antigen markers by determination of the appropriatecombination of different anti-cancer antibodies, to find the mosteffective in targeting and inhibiting growth and development of thetumors.

In all, this invention teaches the use of the AR53A10.11 antigen as atarget for a therapeutic agent, that when administered can reduce thetumor burden of a cancer expressing the antigen in a mammal. Thisinvention also teaches the use of CDMAB (AR53A10.11), and theirderivatives, and antigen binding fragments thereof, and cellularcytotoxicity inducing ligands thereof, to target their antigen to reducethe tumor burden of a cancer expressing the antigen in a mammal.Furthermore, this invention also teaches the use of detecting theAR53A10.11 antigen in cancerous cells that can be useful for thediagnosis, prediction of therapy, and prognosis of mammals bearingtumors that express this antigen.

Accordingly, it is an objective of the invention to utilize a method forproducing cancerous disease modifying antibodies (CDMAB) raised againstcancerous cells derived from a particular individual, or one or moreparticular cancer cell lines, which CDMAB are cytotoxic with respect tocancer cells while simultaneously being relatively non-toxic tonon-cancerous cells, in order to isolate hybridoma cell lines and thecorresponding isolated monoclonal antibodies and antigen bindingfragments thereof for which said hybridoma cell lines are encoded.

It is an additional objective of the invention to teach cancerousdisease modifying antibodies, ligands and antigen binding fragmentsthereof.

It is a further objective of the instant invention to produce cancerousdisease modifying antibodies whose cytotoxicity is mediated throughantibody dependent cellular toxicity.

It is yet an additional objective of the instant invention to producecancerous disease modifying antibodies whose cytotoxicity is mediatedthrough complement dependent cellular toxicity.

It is still a further objective of the instant invention to producecancerous disease modifying antibodies whose cytotoxicity is a functionof their ability to catalyze hydrolysis of cellular chemical bonds.

A still further objective of the instant invention is to producecancerous disease modifying antibodies which are useful for in a bindingassay for diagnosis, prognosis, and monitoring of cancer.

Other objects and advantages of this invention will become apparent fromthe following description wherein are set forth, by way of illustrationand example, certain embodiments of this invention.

BRIEF DESCRIPTION OF THE FIGURES

The patent or application file contains at least one drawing executed incolor. Copies of this patent or patent application publication withcolor drawing(s) will be provided by the Office upon request and paymentof the necessary fee.

FIG. 1 compares the percentage cytotoxicity and binding levels of thehybridoma supernatants against cell lines OCC-1, OVCAR-3 and CCD-27sk.

FIG. 2 represents binding of AR53A10.11 and the anti-EGFR control tocancer and normal cell lines. The data is tabulated to present the meanfluorescence intensity as a fold increase above isotype control.

FIG. 3 includes representative FACS histograms of AR53A10.11 andanti-EGFR antibodies directed against several cancer and non-cancer celllines.

FIG. 4 demonstrates the effect of AR53A10.11 on tumor growth in aprophylactic DLD-1 colon cancer model. The vertical dashed linesindicate the period during which the antibody was administered. Datapoints represent the mean ±SEM.

FIG. 5 demonstrates the effect of AR53A10.11 on body weight in aprophylactic DLD-1 colon cancer model. Data points represent the mean±SEM.

FIG. 6 is a comparison of AR53A10.11 versus positive and negativecontrols on a human tissue microarray.

FIG. 7. Representative micrographs showing the binding pattern on colontumor tissue obtained with AR53A10.11 (A) or the isotype controlantibody (B) and on colon normal tissue obtained with AR53A10.11 (C) oranti-actin (D) from a human tissue microarray. AR53A10.11 displayedstrong positive staining for the tumor cells and negative staining onthe normal tissue. Magnification is 200×.

DETAILED DESCRIPTION OF THE INVENTION

In general, the following words or phrases have the indicated definitionwhen used in the summary, description, examples, and claims.

The term “antibody” is used in the broadest sense and specificallycovers, for example, single monoclonal antibodies (including agonist,antagonist, and neutralizing antibodies, de-immunized, murine, chimericor humanized antibodies), antibody compositions with polyepitopicspecificity, single-chain antibodies, diabodies, triabodies,immunoconjugates and antibody fragments (see below).

The term “monoclonal antibody” as used herein refers to an antibodyobtained from a population of substantially homogeneous antibodies,i.e., the individual antibodies comprising the population are identicalexcept for possible naturally occurring mutations that may be present inminor amounts. Monoclonal antibodies are highly specific, being directedagainst a single antigenic site. Furthermore, in contrast to polyclonalantibody preparations which include different antibodies directedagainst different determinants (epitopes), each monoclonal antibody isdirected against a single determinant on the antigen. In addition totheir specificity, the monoclonal antibodies are advantageous in thatthey may be synthesized uncontaminated by other antibodies. The modifier“monoclonal” indicates the character of the antibody as being obtainedfrom a substantially homogeneous population of antibodies, and is not tobe construed as requiring production of the antibody by any particularmethod. For example, the monoclonal antibodies to be used in accordancewith the present invention may be made by the hybridoma (murine orhuman) method first described by Kohler et al., Nature, 256:495 (1975),or may be made by recombinant DNA methods (see, e.g., U.S. Pat. No.4,816,567). The “monoclonal antibodies” may also be isolated from phageantibody libraries using the techniques described in Clackson et al.,Nature, 352:624-628 (1991) and Marks et al., J. Mol. Biol., 222:581-597(1991), for example.

“Antibody fragments” comprise a portion of an intact antibody,preferably comprising the antigen-binding or variable region thereof.Examples of antibody fragments include less than full length antibodies,Fab, Fab′, F(ab′)₂, and Fv fragments; diabodies; linear antibodies;single-chain antibody molecules; single-chain antibodies, single domainantibody molecules, fusion proteins, recombinant proteins andmultispecific antibodies formed from antibody fragment(s).

An “intact” antibody is one which comprises an antigen-binding variableregion as well as a light chain constant domain (C_(L)) and heavy chainconstant domains, C_(H)1, C_(H)2 and C_(H)3. The constant domains may benative sequence constant domains (e.g. human native sequence constantdomains) or amino acid sequence variant thereof. Preferably, the intactantibody has one or more effector functions.

Depending on the amino acid sequence of the constant domain of theirheavy chains, intact antibodies can be assigned to different “classes”.There are five-major classes of intact antibodies: IgA, IgD, IgE, IgG,and IgM, and several of these may be further divided into “subclasses”(isotypes), e.g., IgG1, IgG2, IgG3, IgG4, IgA, and IgA2. The heavy-chainconstant domains that correspond to the different classes of antibodiesare called a, d, e, ?, and μ, respectively. The subunit structures andthree-dimensional configurations of different classes of immunoglobulinsare well known.

Antibody “effector functions” refer to those biological activitiesattributable to the Fc region (a native sequence Fc region or amino acidsequence variant Fc region) of an antibody. Examples of antibodyeffector functions include C1q binding; complement dependentcytotoxicity; Fc receptor binding; antibody-dependent cell-mediatedcytotoxicity (ADCC); phagocytosis; down regulation of cell surfacereceptors (e.g. B cell receptor; BCR), etc.

“Antibody-dependent cell-mediated cytotoxicity” and “ADCC” refer to acell-mediated reaction in which nonspecific cytotoxic cells that expressFc receptors (FcRs) (e.g. Natural Killer (NK) cells, neutrophils, andmacrophages) recognize bound antibody on a target cell and subsequentlycause lysis of the target cell. The primary cells for mediating ADCC, NKcells, express Fc?RIII only, whereas monocytes express Fc?RI, Fc?RII andFc?RIII. FcR expression on hematopoietic cells is summarized in Table 3on page 464 of Ravetch and Kinet, Annu. Rev. Immunol 9:457-92 (1991). Toassess ADCC activity of a molecule of interest, an in vitro ADCC assay,such as that described in U.S. Pat. No. 5,500,362 or U.S. Pat. No.5,821,337 may be performed. Useful effector cells for such assaysinclude peripheral blood mononuclear cells (PBMC) and Natural Killer(NK) cells. Alternatively, or additionally, ADCC activity of themolecule of interest may be assessed in vivo, e.g., in a animal modelsuch as that disclosed in Clynes et al. PNAS (USA) 95:652-656 (1998).

“Effector cells” are leukocytes which express one or more FcRs andperform effector functions. Preferably, the cells express at leastFc?RIII and perform ADCC effector function. Examples of human leukocyteswhich mediate ADCC include peripheral blood mononuclear cells (PBMC),natural killer (NK) cells, monocytes, cytotoxic T cells and neutrophils;with PBMCs and NK cells being preferred. The effector cells may beisolated from a native source thereof, e.g. from blood or PBMCs asdescribed herein.

The terms “Fc receptor” or “FcR” are used to describe a receptor thatbinds to the Fc region of an antibody. The preferred FcR is a nativesequence human FcR. Moreover, a preferred FcR is one which binds an IgGantibody (a gamma receptor) and includes receptors of the Fc?RI, Fc?RII,and Fc?RIII subclasses, including allelic variants and alternativelyspliced forms of these receptors. Fc?RII receptors include Fc?RIIA (an“activating receptor”) and Fc?RIIB (an “inhibiting receptor”), whichhave similar amino acid sequences that differ primarily in thecytoplasmic domains thereof. Activating receptor Fc?RIIA contains animmunoreceptor tyrosine-based activation motif (ITAM) in its cytoplasmicdomain. Inhibiting receptor Fc?RIIB contains an immunoreceptortyrosine-based inhibition motif (ITIM) in its cytoplasmic domain. (seereview M. in Daëron, Annu. Rev. Immunol. 15:203-234 (1997)). FcRs arereviewed in Ravetch and Kinet, Annu. Rev. Immunol 9:457-92 (1991); Capelet al., Immunomethods 4:25-34 (1994); and de Haas et al., J. Lab. Clin.Med. 126:330-41 (1995). Other FcRs, including those to be identified inthe future, are encompassed by the term “FcR” herein. The term alsoincludes the neonatal receptor, FcRn, which is responsible for thetransfer of maternal IgGs to the fetus (Guyer et al., J. Immunol.117:587 (1976) and Kim et al., Eur. J. Immunol. 24:2429 (1994)).

“Complement dependent cytotoxicity” or “CDC” refers to the ability of amolecule to lyse a target in the presence of complement. The complementactivation pathway is initiated by the binding of the first component ofthe complement system (C1q) to a molecule (e.g. an antibody) complexedwith a cognate antigen. To assess complement activation, a CDC assay,e.g. as described in Gazzano-Santoro et al., J. Immunol. Methods 202:163(1996), may be performed.

The term “variable” refers to the fact that certain portions of thevariable domains differ extensively in sequence among antibodies and areused in the binding and specificity of each particular antibody for itsparticular antigen. However, the variability is not evenly distributedthroughout the variable domains of antibodies. It is concentrated inthree segments called hypervariable regions both in the light chain andthe heavy chain variable domains. The more highly conserved portions ofvariable domains are called the framework regions (FRs). The variabledomains of native heavy and light chains each comprise four FRs, largelyadopting a β-sheet configuration, connected by three hypervariableregions, which form loops connecting, and in some cases forming part of,the 3-sheet structure. The hypervariable regions in each chain are heldtogether in close proximity by the FRs and, with the hypervariableregions from the other chain, contribute to the formation of theantigen-binding site of antibodies (see Kabat et al., Sequences ofProteins of Immunological Interest, 5th Ed. Public Health Service,National Institutes of Health, Bethesda, Md. (1991)). The constantdomains are not involved directly in binding an antibody to an antigen,but exhibit various effector functions, such as participation of theantibody in antibody dependent cellular cytotoxicity (ADCC).

The term “hypervariable region” when used herein refers to the aminoacid residues of an antibody which are responsible for antigen-binding.The hypervariable region generally comprises amino acid residues from a“complementarity determining region” or “CDR” (e.g. residues 24-34 (L1),50-56 (L2) and 89-97 (L3) in the light chain variable domain and 31-35(H1), 50-65 (H2) and 95-102 (H3) in the heavy chain variable domain;Kabat et al., Sequences of proteins of Immunological Interest, 5th Ed.Public Health Service, National Institutes of Health, Bethesda, Md.(1991)) and/or those residues from a “hypervariable loop” (e.g. residues2632 (L1), 50-52 (L2) and 91-96 (L3) in the light chain variable domainand 26-32 (H1), 53-55 (H2) and 96-101 (H3) in the heavy chain variabledomain; Chothia and Lesk J. Mol. Biol. 196:901-917 (1987)). “FrameworkRegion” or “FR” residues are those variable domain residues other thanthe hypervariable region residues as herein defined. Papain digestion ofantibodies produces two identical antigen-binding fragments, called“Fab” fragments, each with a single antigen-binding site, and a residual“Fc” fragment, whose name reflects its ability to crystallize readily.Pepsin treatment yields an F(ab′)₂ fragment that has two antigen-bindingsites and is still capable of cross-linking antigen.

“Fv” is the minimum antibody fragment which contains a completeantigen-recognition and antigen-binding site. This region consists of adimer of one heavy chain and one light chain variable domain in tight,non-covalent association. It is in this configuration that the threehypervariable regions of each variable domain interact to define anantigen-binding site on the surface of the V_(H)-V_(L) dimer.Collectively, the six hypervariable regions confer antigen-bindingspecificity to the antibody. However, even a single variable domain (orhalf of an Fv comprising only three hypervariable regions specific foran antigen) has the ability to recognize and bind antigen, although at alower affinity than the entire binding site. The Fab fragment alsocontains the constant domain of the light chain and the first constantdomain (CHI) of the heavy chain. Fab′ fragments differ from Fabfragments by the addition of a few residues at the carboxy terminus ofthe heavy chain CH1 domain including one or more cysteines from theantibody hinge region. Fab′-SH is the designation herein for Fab′ inwhich the cysteine residue(s) of the constant domains bear at least onefree thiol group. F(ab′)₂ antibody fragments originally were produced aspairs of Fab′ fragments which have hinge cysteines between them. Otherchemical couplings of antibody fragments are also known.

The “light chains” of antibodies from any vertebrate species can beassigned to one of two clearly distinct types, called kappa (?) andlambda (?), based on the amino acid sequences of their constant domains.

“Single-chain Fv” or “scFv” antibody fragments comprise the V_(H) andV_(L) domains of antibody, wherein these domains are present in a singlepolypeptide chain. Preferably, the Fv polypeptide further comprises apolypeptide linker between the V_(H) and V_(L) domains which enables thescFv to form the desired structure for antigen binding. For a review ofscFv see Plückthun in The Pharmacology of Monoclonal Antibodies, vol.113, Rosenburg and Moore eds., Springer-Verlag, New York, pp. 269-315(1994).

The term “diabodies” refers to small antibody fragments with twoantigen-binding sites, which fragments comprise a variable heavy domain(V_(H)) connected to a variable light domain (V_(L)) in the samepolypeptide chain (V_(H)-V_(L)). By using a linker that is too short toallow pairing between the two domains on the same chain, the domains areforced to pair with the complementary domains of another chain andcreate two antigen-binding sites. Diabodies are described more fully in,for example, EP 404,097; WO 93/11161; and Hollinger et al., Proc. Natl.Acad. Sci. USA, 90:6444-6448 (1993).

The term “triabodies” or “trivalent trimers” refers to the combinationof three single chain antibodies. Triabodies are constructed with theamino acid terminus of a V_(L) or V_(H) domain, i.e., without any linkersequence. A triabody has three Fv heads with the polypeptides arrangedin a cyclic, head-to-tail fashion. A possible conformation of thetriabody is planar with the three binding sites located in a plane at anangle of 120 degrees from one another. Triabodies can be monospecific,bispecific or trispecific.

An “isolated” antibody is one which has been identified and separatedand/or recovered from a component of its natural environment.Contaminant components of its natural environment are materials whichwould interfere with diagnostic or therapeutic uses for the antibody,and may include enzymes, hormones, and other proteinaceous ornonproteinaceous solutes. Isolated antibody includes the antibody insitu within recombinant cells since at least one component of theantibody's natural environment will not be present. Ordinarily, however,isolated antibody will be prepared by at least one purification step.

An antibody “which binds” an antigen of interest is one capable ofbinding that antigen with sufficient affinity such that the antibody isuseful as a therapeutic or diagnostic agent in targeting a cellexpressing the antigen. Where the antibody is one which binds theantigen of interest, it will usually preferentially bind the antigen ofinterest as opposed to other proteins, and does not include incidentalbinding such as non-specific Fc contact, or binding topost-translational modifications common to other antigens and may be onewhich does not significantly cross-react with other proteins. Methods,for the detection of an antibody that binds an antigen of interest, arewell known in the art and can include but are not limited to assays suchas FACS, cell ELISA and Western blot.

As used herein, the expressions “cell”, “cell line”, and “cell culture”are used interchangeably, and all such designations include progeny. Itis also understood that all progeny may not be precisely identical inDNA content, due to deliberate or inadvertent mutations. Mutant progenythat have the same function or biological activity as screened for inthe originally transformed cell are included. It will be clear from thecontext where distinct designations are intended.

“Treatment or treating” refers to both therapeutic treatment andprophylactic or preventative measures, wherein the object is to preventor slow down (lessen) the targeted pathologic condition or disorder.Those in need of treatment include those already with the disorder aswell as those prone to have the disorder or those in whom the disorderis to be prevented. Hence, the mammal to be treated herein may have beendiagnosed as having the disorder or may be predisposed or susceptible tothe disorder.

The terms “cancer” and “cancerous” refer to or describe thephysiological condition in mammals that is typically characterized byunregulated cell growth or death. Examples of cancer include, but arenot limited to, carcinoma, lymphoma, blastoma, sarcoma, and leukemia orlymphoid malignancies. More particular examples of such cancers includesquamous cell cancer (e.g. epithelial squamous cell cancer), lung cancerincluding small-cell lung cancer, non-small cell lung cancer,adenocarcinoma of the lung and squamous carcinoma of the lung, cancer ofthe peritoneum, hepatocellular cancer, gastric or stomach cancerincluding gastrointestinal cancer, pancreatic cancer, glioblastoma,cervical cancer, ovarian cancer, liver cancer, bladder cancer, hepatoma,breast cancer, colon cancer, rectal cancer, colorectal cancer,endometrial or uterine carcinoma, salivary gland carcinoma, kidney orrenal cancer, prostate cancer, vulval cancer, thyroid cancer, hepaticcarcinoma, anal carcinoma, penile carcinoma, as well as head and neckcancer.

A “chemotherapeutic agent” is a chemical compound useful in thetreatment of cancer. Examples of chemotherapeutic agents includealkylating agents such as thiotepa and cyclosphosphamide (CYTOXAN™);alkyl sulfonates such as busulfan, improsulfan and piposulfan;aziridines such as benzodopa, carboquone, meturedopa, and uredopa;ethylenimines and methylamelamines including altretamine,triethylenemelamine, triethylenephosphoramide,triethylenethiophosphoramide and trimethylolomelamine; nitrogen mustardssuch as chlorambucil, chlomaphazine, cholophosphamide, estramustine,ifosfamide, mechlorethamine, mechlorethamine oxide hydrochloride,melphalan, novembichin, phenesterine, prednimustine, trofosfamide,uracil mustard; nitrosureas such as carmustine, chlorozotocin,fotemustine, lomustine, nimustine, ranimustine; antibiotics such asaclacinomysins, actinomycin, authramycin, azaserine, bleomycins,cactinomycin, calicheamicin, carabicin, camomycin, carzinophilin,chromomycins, dactinomycin, daunorubicin, detorubicin,6-diazo-5-oxo-L-norleucine, doxorubicin, epirubicin, esorubicin,idarubicin, marcellomycin, mitomycins, mycophenolic acid, nogalamycin,olivomycins, peplomycin, potfiromycin, puromycin, quelamycin,rodorubicin, streptonigrin, streptozocin, tubercidin, ubenimex,zinostatin, zorubicin; anti-metabolites such as methotrexate and5-fluorouracil (5-FU); folic acid analogues such as denopterin,methotrexate, pteropterin, trimetrexate; purine analogs such asfludarabine, 6-mercaptopurine, thiamiprine, thioguanine; pyrimidineanalogs such as ancitabine, azacitidine, 6-azauridine, carmofur,cytarabine, dideoxyuridine, doxifluridine, enocitabine, floxuridine,5-FU; androgens such as calusterone, dromostanolone propionate,epitiostanol, mepitiostane, testolactone; anti-adrenals such asaminoglutethimide, mitotane, trilostane; folic acid replenisher such asfrolinic acid; aceglatone; aldophosphamide glycoside; aminolevulinicacid; amsacrine; bestrabucil; bisantrene; edatraxate; defofamine;demecolcine; diaziquone; elformithine; elliptinium acetate; etoglucid;gallium nitrate; hydroxyurea; lentinan; lonidamine; mitoguazone;mitoxantrone; mopidamol; nitracrine; pentostatin; phenamet; pirarubicin;podophyllinic acid; 2-ethylhydrazide; procarbazine; PSK®; razoxane;sizofiran; spirogermanium; tenuazonic acid; triaziquone;2,2′,2?-trichlorotriethylamine; urethan; vindesine; dacarbazine;mannomustine; mitobronitol; mitolactol; pipobroman; gacytosine;arabinoside (“Ara-C”); cyclophosphamide; thiotepa; taxanes, e.g.paclitaxel (TAXOL®, Bristol-Myers Squibb Oncology, Princeton, N.J.) anddocetaxel (TAXOTERE®, Aventis, Rhone-Poulenc Rorer, Antony, France);chlorambucil; gemcitabine; 6-thioguanine; mercaptopurine; methotrexate;platinum analogs such as cisplatin and carboplatin; vinblastine;platinum; etoposide (VP-16); ifosfamide; mitomycin C; mitoxantrone;vincristine; vinorelbine; navelbine; novantrone; teniposide; daunomycin;aminopterin; xeloda; ibandronate; CPT-11; topoisomerase inhibitor RFS2000; difluoromethylomithine (DMFO); retinoic acid; esperamicins;capecitabine; and pharmaceutically acceptable salts, acids orderivatives of any of the above. Also included in this definition areanti-hormonal agents that act to regulate or inhibit hormone action ontumors such as anti-estrogens including for example tamoxifen,raloxifene, aromatase inhibiting 4(5)-imidazoles, 4-hydroxytamoxifen,trioxifene, keoxifene, LY117018, onapristone, and toremifene (Fareston);and anti-androgens such as flutamide, nilutamide, bicalutamide,leuprolide, and goserelin; and pharmaceutically acceptable salts, acidsor derivatives of any of the above.

“Mammal” for purposes of treatment refers to any animal classified as amammal, including humans, mice, SCID or nude mice or strains of mice,domestic and farm animals, and zoo, sports, or pet animals, such assheep, dogs, horses, cats, cows, etc. Preferably, the mammal herein ishuman.

“Oligonucleotides” are short-length, single- or double-strandedpolydeoxynucleotides that are chemically synthesized by known methods(such as phosphotriester, phosphite, or phosphoramidite chemistry, usingsolid phase techniques such as described in EP 266,032, published 4 May1988, or via deoxynucleoside H-phosphonate intermediates as described byFroehler et al., Nucl. Acids Res., 14:5399-5407, 1986. They are thenpurified on polyacrylamide gels.

In accordance with the present invention, “humanized” and/or “chimeric”forms of non-human (e.g. murine) immunoglobulins refer to antibodieswhich contain specific chimeric immunoglobulins, immunoglobulin chainsor fragments thereof (such as Fv, Fab, Fab′, F(ab′)₂ or otherantigen-binding subsequences of antibodies) which results in thedecrease of a human anti-mouse antibody (HAMA), human anti-chimericantibody (HACA) or a human anti-human antibody (HAHA) response, comparedto the original antibody, and contain the requisite portions (e.g.CDR(s), antigen binding region(s), variable domain(s) and so on) derivedfrom said non-human immunoglobulin, necessary to reproduce the desiredeffect, while simultaneously retaining binding characteristics which arecomparable to said non-human immunoglobulin. For the most part,humanized antibodies are human immunoglobulins (recipient antibody) inwhich residues from the complementarity determining regions (CDRs) ofthe recipient antibody are replaced by residues from the CDRs of anon-human species (donor antibody) such as mouse, rat or rabbit havingthe desired specificity, affinity and capacity. In some instances, Fvframework region (FR) residues of the human immunoglobulin are replacedby corresponding non-human FR residues. Furthermore, the humanizedantibody may comprise residues which are found neither in the recipientantibody nor in the imported CDR or FR sequences. These modificationsare made to further refine and optimize antibody performance. Ingeneral, the humanized antibody will comprise substantially all of atleast one, and typically two, variable domains, in which all orsubstantially all of the CDR regions correspond to those of a non-humanimmunoglobulin and all or substantially all of the FR residues are thoseof a human immunoglobulin consensus sequence. The humanized antibodyoptimally also will comprise at least a portion of an immunoglobulinconstant region (Fc), typically that of a human immunoglobulin.

“De-immunized” antibodies are immunoglobulins that are non-immunogenic,or less immunogenic, to a given species. De-immunization can be achievedthrough structural alterations to the antibody. Any de-immunizationtechnique known to those skilled in the art can be employed. Onesuitable technique for de-immunizing antibodies is described, forexample, in WO 00/34317 published Jun. 15, 2000.

An antibody which induces “apoptosis” is one which induces programmedcell death by any means, illustrated by but not limited to binding ofannexin V, caspase activity, fragmentation of DNA, cell shrinkage,dilation of endoplasmic reticulum, cell fragmentation, and/or formationof membrane vesicles (called apoptotic bodies).

As used herein “antibody induced cytotoxicity” is understood to mean thecytotoxic effect derived from the hybridoma supernatant or antibodyproduced by the hybridoma deposited with the IDAC as accession number141205-04 which effect is not necessarily related to the degree ofbinding.

Throughout the instant specification, hybridoma cell lines, as well asthe isolated monoclonal antibodies which are produced therefrom, arealternatively referred to by their internal designation, AR53A10.11 orDepository Designation, IDAC 141205-04.

As used herein “antibody-ligand” includes a moiety which exhibitsbinding specificity for at least one epitope of the target antigen, andwhich may be an intact antibody molecule, antibody fragments, and anymolecule having at least an antigen-binding region or portion thereof(i.e., the variable portion of an antibody molecule), e.g., an Fvmolecule, Fab molecule, Fab′ molecule, F(ab′).sub.2 molecule, abispecific antibody, a fusion protein, or any genetically engineeredmolecule which specifically recognizes and binds at least one epitope ofthe antigen bound by the isolated monoclonal antibody produced by thehybridoma cell line designated as IDAC 141205-04 (the IDAC 141205-04antigen).

As used herein “cancerous disease modifying antibodies” (CDMAB) refersto monoclonal antibodies which modify the cancerous disease process in amanner which is beneficial to the patient, for example by reducing tumorburden or prolonging survival of tumor bearing individuals, andantibody-ligands thereof.

A “CDMAB related binding agent”, in its broadest sense, is understood toinclude, but is not limited to, any form of human or non-humanantibodies, antibody fragments, antibody ligands, or the like, whichcompetitively bind to at least one CDMAB target epitope.

A “competitive binder” is understood to include any form of human ornon-human antibodies, antibody fragments, antibody ligands, or the likewhich has binding affinity for at least one CDMAB target epitope.

Tumors to be treated include primary tumors and metastatic tumors, aswell as refractory tumors. Refractory tumors include tumors that fail torespond or are resistant to treatment with chemotherapeutic agentsalone, antibodies alone, radiation alone or combinations thereof.Refractory tumors also encompass tumors that appear to be inhibited bytreatment with such agents but recur up to five years, sometimes up toten years or longer after treatment is discontinued.

Tumors that can be treated include tumors that are not vascularized, ornot yet substantially vascularized, as well as vascularized tumors.Examples of solid tumors, which can be accordingly treated, includebreast carcinoma, lung carcinoma, colorectal carcinoma, pancreaticcarcinoma, glioma and lymphoma. Some examples of such tumors includeepidermoid tumors, squamous tumors, such as head and neck tumors,colorectal tumors, prostate tumors, breast tumors, lung tumors,including small cell and non-small cell lung tumors, pancreatic tumors,thyroid tumors, ovarian tumors, and liver tumors. Other examples includeKaposi's sarcoma, CNS neoplasms, neuroblastomas, capillaryhemangioblastomas, meningiomas and cerebral metastases, melanoma,gastrointestinal and renal carcinomas and sarcomas, rhabdomyosarcoma,glioblastoma, preferably glioblastoma multiforme, and leiomyosarcoma.

As used herein “antigen-binding region” means a portion of the moleculewhich recognizes the target antigen.

As used herein “competitively inhibits” means being able to recognizeand bind a determinant site to which the monoclonal antibody produced bythe hybridoma cell line designated as IDAC 141205-04, (the IDAC141205-04 antibody) is directed using conventional reciprocal antibodycompetition assays. (Belanger L., Sylvestre C. and Dufour D. (1973),Enzyme linked immunoassay for alpha fetoprotein by competitive andsandwich procedures. Clinica Chimica Acta 48, 15).

As used herein “target antigen” is. the IDAC 141205-04 antigen orportions thereof.

As used herein, an “immunoconjugate” means any molecule or CDMAB such asan antibody chemically or biologically linked to cytotoxins, radioactiveagents, cytokines, interferons, target or reporter moieties, enzymes,toxins, anti-tumor drugs or therapeutic agents. The antibody or CDMABmay be linked to the cytotoxin, radioactive agent, cytokine, interferon,target or reporter moiety, enzyme, toxin, anti-tumor drug or therapeuticagent at any location along the molecule so long as it is able to bindits target. Examples of immunoconjugates include antibody toxin chemicalconjugates and antibody-toxin fusion proteins.

Radioactive agents suitable for use as anti-tumor agents are known tothose skilled in the art. For example, 131I or 211At is used. Theseisotopes are attached to the antibody using conventional techniques(e.g. Pedley et al., Br. J. Cancer 68, 69-73 (1993)). Alternatively, theanti-tumor agent which is attached to the antibody is an enzyme whichactivates a prodrug. A prodrug may be administered which will remain inits inactive form until it reaches the tumor site where it is convertedto its cytotoxin form once the antibody complex is administered. Inpractice, the antibody-enzyme conjugate is administered to the patientand allowed to localize in the region of the tissue to be treated. Theprodrug is then administered to the patient so that conversion to thecytotoxic drug occurs in the region of the tissue to be treated.Alternatively, the anti-tumor agent conjugated to the antibody is acytokine such as interleukin-2 (IL-2), interleukin-4 (IL-4) or tumornecrosis factor alpha (TNF-a). The antibody targets the cytokine to thetumor so that the cytokine mediates damage to or destruction of thetumor without affecting other tissues. The cytokine is fused to theantibody at the DNA level using conventional recombinant DNA techniques.Interferons may also be used.

As used herein, a “fusion protein” means any chimeric protein wherein anantigen binding region is connected to a biologically active molecule,e.g., toxin, enzyme, fluorescent proteins, luminescent marker,polypeptide tag, cytokine, interferon, target or reporter moiety orprotein drug.

The invention further contemplates CDMAB of the present invention towhich target or reporter moieties are linked. Target moieties are firstmembers of binding pairs. Anti-tumor agents, for example, are conjugatedto second members of such pairs and are thereby directed to the sitewhere the antigen-binding protein is bound. A common example of such abinding pair is avidin and biotin. In a preferred embodiment, biotin isconjugated to the target antigen of the CDMAB of the present invention,and thereby provides a target for an anti-tumor agent or other moietywhich is conjugated to avidin or streptavidin. Alternatively, biotin oranother such moiety is linked to the target antigen of the CDMAB of thepresent invention and used as a reporter, for example in a diagnosticsystem where a detectable signal-producing agent is conjugated to avidinor streptavidin.

Detectable signal-producing agents are useful in vivo and in vitro fordiagnostic purposes. The signal producing agent produces a measurablesignal which is detectable by external means, usually the measurement ofelectromagnetic radiation. For the most part, the signal producing agentis an enzyme or chromophore, or emits light by fluorescence,phosphorescence or chemiluminescence. Chromophores include dyes whichabsorb light in the ultraviolet or visible region, and can be substratesor degradation products of enzyme catalyzed reactions.

Moreover, included within the scope of the present invention is use ofthe present CDMAB in vivo and in vitro for investigative or diagnosticmethods, which are well known in the art. In order to carry out thediagnostic methods as contemplated herein, the instant invention mayfurther include kits, which contain CDMAB of the present invention. Suchkits will be useful for identification of individuals at risk forcertain type of cancers by detecting over-expression of the CDMAB'starget antigen on cells of such individuals.

Diagnostic Assay Kits

It is contemplated to utilize the CDMAB of the present invention in theform of a diagnostic assay kit for determining the presence of a tumor.The tumor will generally be detected in a patient based on the presenceof one or more tumor-specific antigens, e.g. proteins and/orpolynucleotides which encode such proteins in a biological sample, suchas blood, sera, urine and/or tumor biopsies, which samples will havebeen obtained from the patient.

The proteins function as markers which indicate the presence or absenceof a particular tumor, for example a colon, breast, lung or prostatetumor. It is further contemplated that the antigen will have utility forthe detection of other cancerous tumors. Inclusion in the diagnosticassay kits of binding agents comprised of CDMABs of the presentinvention, or CDMAB related binding agents, enables detection of thelevel of antigen that binds to the agent in the biological sample.Polynucleotide primers and probes may be used to detect the level ofmRNA encoding a tumor protein, which is also indicative of the presenceor absence of a cancer. In order for the binding assay to be diagnostic,data will have been generated which correlates statistically significantlevels of antigen, in relation to that present in normal tissue, so asto render the recognition of binding definitively diagnostic for thepresence of a cancerous tumor. It is contemplated that a plurality offormats will be useful for the diagnostic assay of the presentinvention, as are known to those of ordinary skill in the art, for usinga binding agent to detect polypeptide markers in a sample. For example,as illustrated in Harlow and Lane, Antibodies: A Laboratory Manual, ColdSpring Harbor Laboratory, 1988. Further contemplated are any and allcombinations, permutations or modifications of the afore-describeddiagnostic assay formats.

The presence or absence of a cancer in a patient will typically bedetermined by (a) contacting a biological sample obtained from a patientwith a binding agent; (b) detecting in the sample a level of polypeptidethat binds to the binding agent; and (c) comparing the level ofpolypeptide with a predetermined cut-off value.

In an illustrative embodiment, it is contemplated that the assay willinvolve the use of a CDMAB based binding agent immobilized on a solidsupport to bind to and remove the polypeptide from the remainder of thesample. The bound polypeptide may then be detected using a detectionreagent that contains a reporter group and specifically binds to thebinding agent/polypeptide complex. Illustrative detection reagents mayinclude a CDMAB based binding agent that specifically binds to thepolypeptide or an antibody or other agent that specifically binds to thebinding agent, such as an anti-immunoglobulin, protein G, protein A or alectin. In an alternative embodiment, it is contemplated that acompetitive assay may be utilized, in which a polypeptide is labeledwith a reporter group and allowed to bind to the immobilized bindingagent after incubation of the binding agent with the sample. Indicativeof the reactivity of the sample with the immobilized binding agent, isthe extent to which components of the sample inhibit the binding of thelabeled polypeptide to the binding agent. Suitable polypeptides for usewithin such assays include full length tumor-specific proteins and/orportions thereof, to which the binding agent has binding affinity.

The diagnostic kit will be provided with a solid support which may be inthe form of any material known to those of ordinary skill in the art towhich the protein may be attached. Suitable examples may include a testwell in a microtiter plate or a nitrocellulose or other suitablemembrane. Alternatively, the support may be a bead or disc, such asglass, fiberglass, latex or a plastic material such as polystyrene orpolyvinylchloride. The support may also be a magnetic particle or afiber optic sensor, such as those disclosed, for example, in U.S. Pat.No. 5,359,681.

It is contemplated that the binding agent will be immobilized on thesolid support using a variety of techniques known to those of skill inthe art, which are amply described in the patent and scientificliterature. The term “immobilization” refers to both noncovalentassociation, such as adsorption, and covalent attachment, which, in thecontext of the present invention, may be a direct linkage between theagent and functional groups on the support, or may be a linkage by wayof a cross-linking agent. In a preferred, albeit non-limitingembodiment, immobilization by adsorption to a well in a microtiter plateor to a membrane is preferable. Adsorption may be achieved by contactingthe binding agent, in a suitable buffer, with the solid support for asuitable amount of time. The contact time may vary with temperature, andwill generally be within a range of between about 1 hour and about 1day.

Covalent attachment of binding agent to a solid support would ordinarilybe accomplished by first reacting the support with a bifunctionalreagent that will react with both the support and a functional group,such as a hydroxyl or amino group, on the binding agent. For example,the binding agent may be covalently attached to supports having anappropriate polymer coating using benzoquinone or by condensation of analdehyde group on the support with an amine and an active hydrogen onthe binding partner (see, e.g., Pierce Immunotechnology Catalog andHandbook, 1991, at A12 A13).

It is further contemplated that the diagnostic assay kit will take theform of a two-antibody sandwich assay. This assay may be performed byfirst contacting an antibody, e.g. the instantly disclosed CDMAB thathas been immobilized on a solid support, commonly the well of amicrotiter plate, with the sample, such that polypeptides within thesample are allowed to bind to the immobilized antibody. Unbound sampleis then removed from the immobilized polypeptide-antibody complexes anda detection reagent (preferably a second antibody capable of binding toa different site on the polypeptide) containing a reporter group isadded. The amount of detection reagent that remains bound to the solidsupport is then determined using a method appropriate for the specificreporter group.

In a specific embodiment, it is contemplated that once the antibody isimmobilized on the support as described above, the remaining proteinbinding sites on the support will be blocked, via the use of anysuitable blocking agent known to those of ordinary skill in the art,such as bovine serum albumin or Tween 20™ (Sigma Chemical Co., St.Louis, Mo.). The immobilized antibody would then be incubated with thesample, and polypeptide would be allowed to bind to the antibody. Thesample could be diluted with a suitable diluent, such asphosphate-buffered saline (PBS) prior to incubation. In general, anappropriate contact time (i.e., incubation time) would be selected tocorrespond to a period of time sufficient to detect the presence ofpolypeptide within a sample obtained from an individual with thespecifically selected tumor. Preferably, the contact time is sufficientto achieve a level of binding that is at least about 95 percent of thatachieved at equilibrium between bound and unbound polypeptide. Those ofordinary skill in the art will recognize that the time necessary toachieve equilibrium may be readily determined by assaying the level ofbinding that occurs over a period of time.

It is further contemplated that unbound sample would then be removed bywashing the solid support with an appropriate buffer. The secondantibody, which contains a reporter group, would then be added to thesolid support. Incubation of the detection reagent with the immobilizedantibody-polypeptide complex would then be carried out for an amount oftime sufficient to detect the bound polypeptide. Subsequently, unbounddetection reagent would then be removed and bound detection reagentwould be detected using the reporter group. The method employed fordetecting the reporter group is necessarily specific to the type ofreporter group selected, for example for radioactive groups,scintillation counting or autoradiographic methods are generallyappropriate. Spectroscopic methods may be used to detect dyes,luminescent groups and fluorescent groups. Biotin may be detected usingavidin, coupled to a different reporter group (commonly a radioactive orfluorescent group or an enzyme). Enzyme reporter groups may generally bedetected by the addition of substrate (generally for a specific periodof time), followed by spectroscopic or other analysis of the reactionproducts.

In order to utilize the diagnostic assay kit of the present invention todetermine the presence or absence of a cancer, such as prostate cancer,the signal detected from the reporter group that remains bound to thesolid support would generally be compared to a signal that correspondsto a predetermined cut-off value. For example, an illustrative cut-offvalue for the detection of a cancer may be the average mean signalobtained when the immobilized antibody is incubated with samples frompatients without the cancer. In general, a sample generating a signalthat is about three standard deviations above the predetermined cut-offvalue would be considered positive for the cancer. In an alternateembodiment, the cut-off value might be determined by using a ReceiverOperator Curve, according to the method of Sackett et al., ClinicalEpidemiology. A Basic Science for Clinical Medicine, Little Brown andCo., 1985, p. 106-7. In such an embodiment, the cut-off value could bedetermined from a plot of pairs of true positive rates (i.e.,sensitivity) and false positive rates (100 percent-specificity) thatcorrespond to each possible cut-off value for the diagnostic testresult. The cut-off value on the plot that is the closest to the upperleft-hand corner (i.e., the value that encloses the largest area) is themost accurate cut-off value, and a sample generating a signal that ishigher than the cut-off value determined by this method may beconsidered positive. Alternatively, the cut-off value may be shifted tothe left along the plot, to minimize the false positive rate, or to theright, to minimize the false negative rate. In general, a samplegenerating a signal that is higher than the cut-off value determined bythis method is considered positive for a cancer.

It is contemplated that the diagnostic assay enabled by the kit will beperformed in either a flow-through or strip test format, wherein thebinding agent is immobilized on a membrane, such as nitrocellulose. Inthe flow-through test, polypeptides within the sample bind to theimmobilized binding agent as the sample passes through the membrane. Asecond, labeled binding agent then binds to the bindingagent-polypeptide complex as a solution containing the second bindingagent flows through the membrane. The detection of bound second bindingagent may then be performed as described above. In the strip testformat, one end of the membrane to which binding agent is bound will beimmersed in a solution containing the sample. The sample migrates alongthe membrane through a region containing second binding agent and to thearea of immobilized binding agent. Concentration of the second bindingagent at the area of immobilized antibody indicates the presence of acancer. Generation of a pattern, such as a line, at the binding site,which can be read visually, will be indicative of a positive test. Theabsence of such a pattern indicates a negative result. In general, theamount of binding agent immobilized on the membrane is selected togenerate a visually discernible pattern when the biological samplecontains a level of polypeptide that would be sufficient to generate apositive signal in the two-antibody sandwich assay, in the formatdiscussed above. Preferred binding agents for use in the instantdiagnostic assay are the instantly disclosed antibodies, antigen-bindingfragments thereof, and any CDMAB related binding agents as hereindescribed. The amount of antibody immobilized on the membrane will beany amount effective to produce a diagnostic assay, and may range fromabout 25 nanograms to about 1 microgram. Typically such tests may beperformed with a very small amount of biological sample.

Additionally, the CDMAB of the present invention may be used in thelaboratory for research due to its ability to identify its targetantigen.

In order that the invention herein described may be more fullyunderstood; the following description is set forth.

The present invention provides CDMAB (i.e., IDAC 141205-04 CDMAB) whichspecifically recognize and bind the IDAC 141205-04 antigen.

The CDMAB of the isolated monoclonal antibody produced by the hybridomadeposited with the IDAC as accession number 141205-04 may be in any formas long as it has an antigen-binding region which competitively inhibitsthe immunospecific binding of the isolated monoclonal antibody producedby hybridoma IDAC 141205-04 to its target antigen. Thus, any recombinantproteins (e.g., fusion proteins wherein the antibody is combined with asecond protein such as a lymphokine or a tumor inhibitory growth factor)having the same binding specificity as the IDAC 141205-04 antibody fallwithin the scope of this invention.

In one embodiment of the invention, the CDMAB is the IDAC 141205-04antibody.

In other embodiments, the CDMAB is an antigen binding fragment which maybe a Fv molecule (such as a single-chain Fv molecule), a Fab molecule, aFab′ molecule, a F(ab′)2 molecule, a fusion protein, a bispecificantibody, a heteroantibody or any recombinant molecule having theantigen-binding region of the IDAC 141205-04 antibody. The CDMAB of theinvention is directed to the epitope to which the IDAC 141205-04monoclonal antibody is directed.

The CDMAB of the invention may be modified, i.e., by amino acidmodifications within the molecule, so as to produce derivativemolecules. Chemical modification may also be possible. Modification bydirect mutation, methods of affinity maturation, phage display or chainshuffling may also be possible.

Affinity and specificity can be modified or improved by mutating CDRand/or phenylalanine tryptophan (FW) residues and screening for antigenbinding sites having the desired characteristics (e.g., Yang et al., J.Mol. Biol., (1995) 254: 392-403). One way is to randomize individualresidues or combinations of residues so that in a population ofotherwise identical antigen binding sites, subsets of from two to twentyamino acids are found at particular positions. Alternatively, mutationscan be induced over a range of residues by error prone PCR methods(e.g., Hawkins et al., J. Mol. Biol., (1992) 226: 889-96). In anotherexample, phage display vectors containing heavy and light chain variableregion genes can be propagated in mutator strains of E. coli (e.g., Lowet al., J. Mol. Biol., (1996) 250: 359-68). These methods of mutagenesisare illustrative of the many methods known to one of skill in the art.

Another manner for increasing affinity of the antibodies of the presentinvention is to carry out chain shuffling, where the heavy or lightchain are randomly paired with other heavy or light chains to prepare anantibody with higher affinity. The various CDRs of the antibodies mayalso be shuffled with the corresponding CDRs in other antibodies.

Derivative molecules would retain the functional property of thepolypeptide, namely, the molecule having such substitutions will stillpermit the binding of the polypeptide to the IDAC 141205-04 antigen orportions thereof.

These amino acid substitutions include, but are not necessarily limitedto, amino acid substitutions known in the art as “conservative”.

For example, it is a well-established principle of protein chemistrythat certain amino acid substitutions, entitled “conservative amino acidsubstitutions,” can frequently be made in a protein without alteringeither the conformation or the function of the protein.

Such changes include substituting any of isoleucine (I), valine (V), andleucine (L) for any other of these hydrophobic amino acids; asparticacid (D) for glutamic acid (E) and vice versa; glutamine (Q) forasparagine (N) and vice versa; and serine (S) for threonine (T) and viceversa. Other substitutions can also be considered conservative,depending on the environment of the particular amino acid and its rolein the three-dimensional structure of the protein. For example, glycine(G) and alanine (A) can frequently be interchangeable, as can alanineand valine (V). Methionine (M), which is relatively hydrophobic, canfrequently be interchanged with leucine and isoleucine, and sometimeswith valine. Lysine (K) and arginine (R) are frequently interchangeablein locations in which the significant feature of the amino acid residueis its charge and the differing pK's of these two amino acid residuesare not significant. Still other changes can be considered“conservative” in particular environments.

EXAMPLE 1

Hybridoma Production—Hybridoma Cell Line AR53A10.11

The hybridoma cell line AR53A10.11 was deposited, in accordance with theBudapest Treaty, with the International Depository Authority of Canada(IDAC), Bureau of Microbiology, Health Canada, 1015 Arlington Street,Winnipeg, Manitoba, Canada, R3E 3R2, on Dec. 14, 2005, under AccessionNumber 141205-04. In accordance with 37 CFR 1.808, the depositors assurethat all restrictions imposed on the availability to the public of thedeposited materials will be irrevocably removed upon the granting of apatent.

To produce the hybridoma that produces the anti-cancer antibodyAR53A10.11, a single cell suspension of frozen human prostate tumortissue (Genomics Collaborative, Cambridge, Mass.) was prepared in PBS.IMMUNEASY™ (Qiagen, Venlo, Netherlands) adjuvant was prepared for use bygentle mixing. Five to seven week old BALB/c mice were immunized byinjecting subcutaneously, 2 million cells in 50 microliters of theantigen-adjuvant. Recently prepared antigen-adjuvant was used to boostthe immunized mice intraperitoneally, 2 and 5 weeks after the initialimmunization, with 2 million cells in 50 microliters. A spleen was usedfor fusion three days after the last immunization. The hybridomas wereprepared by fusing the isolated splenocytes with NSO-1 myeloma partners.The supernatants from the fusions were tested from subclones of thehybridomas.

To determine whether the antibodies secreted by the hybridoma cells areof the IgG or IgM isotype, an ELISA assay was employed. 100microliters/well of goat anti-mouse IgG+IgM (H+L) at a concentration of2.4 micrograms/mL in coating buffer (0.1 M carbonate/bicarbonate buffer,pH 9.2-9.6) at 4° C. was added to the ELISA plates overnight. The plateswere washed thrice in washing buffer (PBS+0.05 percent Tween-20). 100microliters/well blocking buffer (5 percent milk in wash buffer) wasadded to the plate for 1 hour at room temperature and then washed thricein washing buffer. 100 microliters/well of hybridoma supernatant wasadded and the plate incubated for 1 hour at room temperature. The plateswere washed thrice with washing buffer and 1/100,000 dilution of eithergoat anti-mouse IgG or IgM horseradish peroxidase conjugate (diluted inPBS containing 1 percent milk), 100 microliters/well, was added. Afterincubating the plate for 1 hour at room temperature the plate was washedthrice with washing buffer. 100 microliters/well of TMB solution wasincubated for 1-3 minutes at room temperature. The color reaction wasterminated by adding 50 microliters/well 2M H₂S0₄ and the plate was readat 450 nm with a Perkin-Elmer HTS7000 plate reader. As indicated in FIG.1, the AR53A10.11 hybridoma secreted primarily antibodies of the IgGisotype.

To determine the subclass of antibody secreted by the hybridoma cells,an isotyping experiment was performed using a Mouse Monoclonal AntibodyIsotyping Kit (HyCult Biotechnology, Frontstraat, Netherlands). 500microliters of buffer solution was added to the test strip containingrat anti-mouse subclass specific antibodies. 500 microliters ofhybridoma supernatant was added to the test tube, and submerged bygentle agitation. Captured mouse immunoglobulins were detected directlyby a second rat monoclonal antibody which is coupled to colloidparticles. The combination of these two proteins creates a visual signalused to analyse the isotype. The anti-cancer antibody AR53A10.11 is ofthe IgG2b, kappa isotype.

After one round of limiting dilution, hybridoma supernatants were testedfor antibodies that bound to target cells in a cell ELISA assay. Twohuman ovarian cancer cell lines and 1 human normnal skin cell line weretested: OCC-1, OVCAR-3, and CCD-27sk respectively. The cell lines,except for the OCC-1 ovarian cancer cell line, were obtained from theAmerican Type Tissue Collection (ATCC, Manassas, Va.). OCC-1 ovariancancer cell line was obtained from the Ottawa Regional Cancer Center(Ottawa, ON).

The plated cells were fixed prior to use. The plates were washed thricewith PBS containing MgCl₂ and CaCl₂ at room temperature. 100 microlitersof 2 percent paraformaldehyde diluted in PBS was added to each well for10 minutes at room temperature and then discarded. The plates were againwashed with PBS containing MgCl₂ and CaCl₂ three times at roomtemperature. Blocking was done with 100 microliters/well of 5 percentmilk in wash buffer (PBS+0.05 percent Tween-20) for 1 hour at roomtemperature. The plates were washed thrice with wash buffer and thehybridoma supernatant was added at 100 microliters/well for 1 hour atroom temperature. The plates were washed 3 times with wash buffer and100 microliters/well of 1/25,000 dilution of goat anti-mouse IgGantibody conjugated to horseradish peroxidase (diluted in PBS containing1 percent milk) was added. After 1 hour incubation at room temperaturethe plates were washed 3 times with wash buffer and 100 microliter/wellof TMB substrate was incubated for 1-3 minutes at room temperature. Thereaction was terminated with 50 microliters/well 2M H₂S0₄ and the plateread at 450 nm with a Perkin-Elmer HTS7000 plate reader. The results astabulated in FIG. 1 were expressed as the number of folds abovebackground compared to an in-house IgG isotype control that haspreviously been shown not to bind to the cell lines tested. Theantibodies from the hybridoma AR53A10.11 showed no detectable binding tothe cell lines tested.

In conjunction with testing for antibody binding, the cytotoxic effectof the hybridoma supernatants was tested in the cell lines: OCC-1,OVCAR-3, and CCD-27sk. Calcein AM was obtained from Molecular Probes(Eugene, Oreg.). The assays were performed according to themanufacturer's instructions with the changes outlined below. Cells wereplated before the assay at the predetermined appropriate density. After2 days, 100 microliters of supernatant from the hybridoma microtiterplates were transferred to the cell plates and incubated in a 5 percentCO₂ incubator for 5 days. The wells that served as the positive controlswere aspirated until empty and 100 microliters of sodium azide (NaN₃) orcycloheximide was added. After 5 days of treatment, the plates were thenemptied by inverting and blotting dry. Room temperature DPBS (Dulbecco'sphosphate buffered saline) containing MgCl₂ and CaCl₂ was dispensed intoeach well from a multichannel squeeze bottle, tapped 3 times, emptied byinversion and then blotted dry. 50 microliters of the fluorescentcalcein dye diluted in DPBS containing MgCl₂ and CaCl₂ was added to eachwell and incubated at 37° C. in a 5 percent CO₂ incubator for 30minutes. The plates were read in a Perkin-Elmer HTS7000 fluorescenceplate reader and the data was analyzed in Microsoft Excel. The resultsare tabulated in FIG. 1. Supernatant from the AR53A10.11 hybridomaproduced specific cytotoxicity of 13 percent on the OCC-1 cells. Thiswas 16 and 14 percent of the cytotoxicity obtained with the positivecontrols sodium azide and cycloheximide, respectively. Specificcytotoxicity of 15 percent was also observed on OVCAR-3 cells. This was25 and 33 percent of the cytotoxicity obtained with the positivecontrols sodium azide and cycloheximide, respectively. Results from FIG.1 demonstrate that the cytotoxic effects of AR53A10.11 are notproportional to the binding levels on the cancer cell types. Astabulated in FIG. 1, AR53A10.11 did not produce cytotoxicity in theCCD-27sk normal cell line. The known non-specific cytotoxic agentscycloheximide and NaN₃ generally produced cytotoxicity as expected.

EXAMPLE 2

In Vitro Binding

AR53A10.11 monoclonal antibody was produced by culturing the hybridomain CL-1000 flasks (BD Biosciences, Oakville, ON) with collections andreseeding occurring twice/week. Standard antibody purificationprocedures with Protein G Sepharose 4 Fast Flow (Amersham Biosciences,Baie d'Urfé, QC) were followed. It is within the scope of this inventionto utilize monoclonal antibodies that are de-immunized, humanized,chimeric or murine.

Binding of AR53A10.11 to colon (SW1116, Lovo and DLD-1), prostate (PC-3and Du-145), pancreatic (PL45, ASPC-1 and BxPC-3), breast (MDA-MB-231,MDA-MB-468 and MCF-7), lung (A549) and ovarian (OV2008, ES-2, Hey,A2780-cp, A2780-s, OCC-1, OVCAR-3, C-13, ES-2 and OVCA-429) cancer, andnon-cancer cell lines from skin (CCD-27sk) and lung (Hs888.Lu) wasassessed by flow cytometry (FACS). All cell lines, except for themajority of the ovarian cancer cell lines, were obtained from theAmerican Type Tissue Collection (ATCC, Manassas, Va.). OV-2008, ES-2,Hey, A2780-cp, A2780-s, OCC-1, C-13 and OVCA-429 ovarian cancer celllines were obtained from the Ottawa Regional Cancer Center (Ottawa, ON).

Cells were prepared for FACS by initially washing the cell monolayerwith DPBS (without Ca⁺⁺ and Mg⁺⁺). Cell dissociation buffer (INVITROGEN,Burlington, ON) was then used to dislodge the cells from their cellculture plates at 37° C. After centrifugation and collection, the cellswere resuspended in DPBS containing MgCl₂, CaCl₂ and 2 percent fetalbovine serum at 4° C. (staining media) and counted, aliquoted toappropriate cell density, spun down to pellet the cells and resuspendedin staining media at 4° C. in the presence of the test antibody(AR53A10.11) or control antibodies (isotype control, anti-EGFR). Isotypecontrol and the test antibody were assessed at 20 micrograms/mL whereasanti-EGFR was assessed at 5 micrograms/mL on ice for 30 minutes. Priorto the addition of Alexa Fluor 546-conjugated secondary antibody thecells were washed once with staining media. The Alexa Fluor546-conjugated antibody in staining media was then added for 30 minutesat 4° C. The cells were then washed for the final time and resuspendedin fixing media (staining media containing 1.5 percentparaformaldehyde). Flow cytometric acquisition of the cells was assessedby running samples on a FACSarray™ using the FACSarray™ System Software(BD Biosciences, Oakville, ON). The forward (FSC) and side scatter (SSC)of the cells were set by adjusting the voltage and amplitude gains onthe FSC and SSC detectors. The detectors for the fluorescence(Alexa-546) channel was adjusted by running unstained cells such thatcells had a uniform peak with a median fluorescent intensity ofapproximately 1-5 units. For each sample, approximately 10,000 gatedevents (stained fixed cells) were acquired for analysis and the resultsare presented in FIG. 3.

FIG. 2 presents the mean fluorescence intensity fold increase aboveisotype control. Representative histograms of AR53A10.11 antibodies werecompiled for FIG. 3. AR53A10.11 showed weak binding to the colon cancercell lines Lovo and DLD-1 (1.6-fold and 1.5-fold respectively) and tothe pancreatic cancer cell line PL45 (2.0-fold). AR53A10.11 did notdemonstrate detectable binding to the other cancer cell lines. Bindingto the CCD-27sk non-cancer skin and Hs888.Lu non-cancer lung cell lineswas not detectable under these conditions. From Examples 1 and 2, it isevident that the binding of AR53A10.11 to the OCC-1 and OVCAR-3 cancercancer cell lines is not detectable using cell ELISA or FACS.Nevertheless, the antibody was able to induce a cytotoxic effect inthese cell lines. The effect may be due to the following factor. It ispossible that the OCC-1/OVCAR-3 ovarian cancer cell line expresses theantigen target at a level below the threshold of detection by thismethod under these conditions, but that the low level of expression issufficient to trigger an event leading to delayed tumor growth. Thecytotoxic effect of this antibody in an OCC-1 and OVCAR-3 ovarian cancermodel is a non-obvious finding that could not have been predicted on thebasis of binding.

EXAMPLE 3

In Vivo Tumor Experiments with DLD-1 Cells

Examples 1 and 2 demonstrated that AR53A10.11 had anti-cancer propertiesagainst human cancer cell lines with detectable binding against colonand pancreatic cancer indications. With reference to FIGS. 4 and 5, 4 to6 week old female SCID mice were implanted with 5 million human coloncancer cells (DLD-1) in 100 microliters saline injected subcutaneouslyin the scruff of the neck. The mice were randomly divided into 2treatment groups of 5. On the day after implantation, 20 mg/kg ofAR53A10.11 test antibody or buffer control was administeredintraperitoneally to each cohort in a volume of 300 microliters afterdilution from the stock concentration with a diluent that contained 2.7mM KCl, 1 mM KH₂PO₄, 137 mM NaCl and 20 mM Na₂HPO₄. The antibody andcontrol samples were then administered once per week for the duration ofthe study in the same fashion. Tumor growth was measured about everyseventh day with calipers. The study was completed after 7 injections(48 days), as the animals reached CCAC end-points due to large ulceratedlesions. Body weights of the animals were recorded once per week for theduration of the study. At the end of the study all animals wereeuthanized according to CCAC guidelines.

AR53A10.11 reduced tumor growth in the highly aggressive DLD-1 in vivoprophylactic model of human colon cancer. On day 48 post-implantation, 5days after the last treatment dose, the mean tumor volume in theAR53A10.11 treated group was 65 percent lower than the tumor volume inthe buffer control-treated group (FIG. 4). The tumor volume at the endof the study was significantly different from that of the control(p=0.019, t-test). Average tumor volumes at the final timepoint wereinfluenced by the loss of mice, especially from the control group, dueto ulcerated lesions before the termination of the treatment period. AtDay 27, when all mice were still alive, AR53A10.11 caused a similar 62percent decrease in tumor volume (p=0.005). This marked decrease wasobserved after only 4 injections of the antibody.

There were no clinical signs of toxicity throughout the study. Bodyweight measured at weekly intervals was a surrogate for well-being andfailure to thrive. As seen in FIG. 5, there were no significantdifferences in the body weights of the control or AR53A10.11-treatedgroups over the course of the study. There was also no difference inbody weight between the two groups at the end of the treatment period(p=0.641, t-test).

Therefore AR53A10.11 was well-tolerated and decreased the tumor burdenin this human colon cancer xenograft model. A treatment benefit wasobserved in a well-recognized colon model of human cancer diseasesuggesting pharmacologic and pharmaceutical benefits of this antibodyfor therapy in other mammals, including man.

EXAMPLE 4

Human Normal and Multi-Tumor Tissue Staining

IHC studies were conducted to characterize the AR53A10.11 antigendistribution in humans. Binding of antibodies to 4 human normal (colon,lung, prostate and breast) and 16 human tumor tissues (4 of colon, lung,prostate and breast) was performed using a human, normal and tumor organtissue screening array (Tri Star, Rockville, Md.).

Slides were postfixed for 10 minutes in cold (−20° C.) acetone and thenallowed to come to room temperature. Slides were rinsed in 4° C. coldphosphate buffered saline (PBS) 3 times for 2 minutes each followed byblocking endogenous peroxidase activity with washing in 3 percenthydrogen peroxide for 10 minutes. Slides were then rinsed in PBS 3 timesfor 5 minutes followed by incubation in Universal blocking solution(Dako, Toronto, Ontario) for 5 minutes at room temperature. AR53A10.11,anti-human muscle actin (Clone HHF35, Dako, Toronto, Ontario) or isotypecontrol antibody (directed towards Aspergillus niger glucose oxidase, anenzyme which is neither present nor inducible in mammalian tissues;Dako, Toronto, Ontario) were diluted in antibody dilution buffer (Dako,Toronto, Ontario) to its working concentration (5 micrograms/mL for eachantibody except for anti-actin which was 0.5 micrograms/mL) andincubated overnight for 1 hour at room temperature. The slides werewashed with PBS 3 times for 2 minutes each. Immunoreactivity of theprimary antibodies was detected/visualized with HRP conjugated secondaryantibodies as supplied (Dako Envision System, Toronto, Ontario) for 30minutes at room temperature. Following this step the slides were washedwith PBS 3 times for 5 minutes each and a color reaction developed byadding DAB (3,3′-diaminobenzidine tetrahydrachloride, Dako, Toronto,Ontario) chromogen substrate solution for immunoperoxidase staining for10 minutes at room temperature. Washing the slides in tap waterterminated the chromogenic reaction. Following counterstaining withMeyer's Hematoxylin (Sigma Diagnostics, Oakville, ON), the slides weredehydrated with graded ethanols (75-100 percent) and cleared withxylene. Using mounting media (Dako Faramount, Toronto, Ontario) theslides were coverslipped. Slides were microscopically examined using anAxiovert 200 (Ziess Canada, Toronto, ON) and digital images acquired andstored using Northern Eclipse Imaging Software (Mississauga, ON).Results were read, scored and interpreted by a histopathologist.

FIG. 6 presents a summary of the results of AR53A10.11 staining of anarray of human normal and tumor tissues. The AR53A10.11 antibody showedbinding to 4/4 of colon (FIG. 7), breast, lung and prostate tumor tissuewith no binding to their corresponding normal tissues with the exceptionof prostate. Within the tissue section, the antibody binding wasrestricted to tumor cells. Cellular localization was both cytoplasmicand membranous. These results suggest that the antigen for AR53A10.11 isexpressed on a variety of tumor types. In addition, the antigen forAR53A10.11 is not widely expressed on normal tissues, suggesting thatthe antibody binds specifically to a limited number of tissues inhumans.

EXAMPLE 5

Isolation of Competitive Binders

Given an antibody, an individual ordinarily skilled in the art cangenerate a competitively inhibiting CDMAB, for example a competingantibody, which is one that recognizes the same epitope (Belanger L etal. Clinica Chimica Acta 48:15-18 (1973)). One method entails immunizingwith an immunogen that expresses the antigen recognized by the antibody.The sample may include but is not limited to tissues, isolatedprotein(s) or cell line(s). Resulting hybridomas could be screened usinga competition assay, which is one that identifies antibodies thatinhibit the binding of the test antibody, such as ELISA, FACS or Westernblotting. Another method could make use of phage display antibodylibraries and panning for antibodies that recognize at least one epitopeof said antigen (Rubinstein J L et al. Anal Biochem 314:294-300 (2003)).In either case, antibodies are selected based on their ability todisplace the binding of the original labeled antibody to at least oneepitope of its target antigen. Such antibodies would therefore possessthe characteristic of recognizing at least one epitope of the antigen asthe original antibody.

EXAMPLE 6

Cloning of the Variable Regions of the AR53A10.11 Monoclonal Antibody

The sequences of the variable regions from the heavy (V_(H)) and light(V_(L)) chains of monoclonal antibody produced by the AR53A10.11hybridoma cell line can be determined. RNA encoding the heavy and lightchains of immunoglobulin can be extracted from the subject hybridomausing standard methods involving cellular solubilization withguanidinium isothiocyanate (Chirgwin et al. Biochem. 18:5294-5299(1979)). The mRNA can be used to prepare cDNA for subsequent isolationof V_(H) and V_(L) genes by PCR methodology known in the art (Sambrooket al., eds., Molecular Cloning, Chapter 14, Cold Spring Harborlaboratories Press, N.Y. (1989)). The N-terminal amino acid sequence ofthe heavy and light chains can be independently determined by automatedEdman sequencing. Further stretches of the CDRs and flanking FRs canalso be determined by amino acid sequencing of the V_(H) and V_(L)fragments. Synthetic primers can be then designed for isolation of theV_(H) and V_(L) genes from AR53A10.11 monoclonal antibody, and theisolated gene can be ligated into an appropriate vector for sequencing.To generate chimeric and humanized IgG, the variable light and variableheavy domains can be subcloned into an appropriate vector forexpression.

In another embodiment, AR53A10.11 or its de-immunized, chimeric orhumanized version is produced by expressing a nucleic acid encoding theantibody in a transgenic animal, such that the antibody is expressed andcan be recovered. For example, the antibody can be expressed in a tissuespecific manner that facilitates recovery and purification. In one suchembodiment, an antibody of the invention is expressed in the mammarygland for secretion during lactation. Transgenic animals include but arenot limited to mice, goat and rabbit.

(i) Monoclonal Antibody

DNA encoding the monoclonal antibody (as outlined in Example 1) isreadily isolated and sequenced using conventional procedures (e.g., byusing oligonucleotide probes that are capable of binding specifically togenes encoding the heavy and light chains of the monoclonal antibodies).The hybridoma cell serves as a preferred source of such DNA. Onceisolated, the DNA may be placed into expression vectors, which are thentransfected into host cells such as E. coli cells, simian COS cells,Chinese hamster ovary (CHO) cells, or myeloma cells that do nototherwise produce immunoglobulin protein, to obtain the synthesis ofmonoclonal antibodies in the recombinant host cells. The DNA also may bemodified, for example, by substituting the coding sequence for humanheavy and light chain constant domains in place of the homologous murinesequences. Chimeric or hybrid antibodies also may be prepared in vitrousing known methods in synthetic protein chemistry, including thoseinvolving crosslinking agents. For example, immunotoxins may beconstructed using a disulfide exchange reaction or by forming athioether bond. Examples of suitable reagents for this purpose includeiminothiolate and methyl-4-mercaptobutyrimidate.

(ii) Humanized Antibody

A humanized antibody has one or more amino acid residues introduced intoit from a non-human source. These non-human amino acid residues areoften referred to as “import” residues, which are typically taken froman “import” variable domain. Humanization can be performed the method ofWinter and co-workers by substituting rodent CDRs or CDR sequences forthe corresponding sequences of a human antibody (Jones et al., Nature321:522-525 (1986); Riechmann et al., Nature 332:323-327 (1988);Verhoeyen et al., Science 239:1534-1536 (1988); reviewed in Clark,Immunol. Today 21:397-402 (2000)).

A humanized antibody can be prepared by a process of analysis of theparental sequences and various conceptual humanized products usingthree-dimensional models of the parental and humanized sequences. Threedimensional immunoglobulin models are commonly available and arefamiliar to those skilled in the art. Computer programs are availablewhich illustrate and display probable three-dimensional conformationalstructures of selected candidate immunoglobulin sequences. Inspection ofthese displays permits analysis of the likely role of the residues inthe functioning of the candidate immunoglobulin sequence, i.e. theanalysis of residues that influence the ability of the candidateimmunoglobulin to bind its antigen. In this way, FR residues can beselected and combined from the consensus and import sequence so that thedesired antibody characteristic, such as increased affinity for thetarget antigen(s), is achieved. In general, the CDR residues aredirectly and most substantially involved in influencing antigen binding.

(iii) Antibody Fragments

Various techniques have been developed for the production of antibodyfragments. These fragments can be produced by recombinant host cells(reviewed in Hudson, Curr. Opin. Immunol. 11:548-557 (1999); Little etal., Immunol. Today 21:364-370 (2000)). For example, Fab′-SH fragmentscan be directly recovered from E. coli and chemically coupled to formF(ab′)₂ fragments (Carter et al., Biotechnology 10:163-167 (1992)). Inanother embodiment, the F(ab′)₂ is formed using the leucine zipper GCN4to promote assembly of the F(ab′)₂ molecule. According to anotherapproach, Fv, Fab or F(ab′)₂ fragments can be isolated directly fromrecombinant host cell culture.

EXAMPLE 7

A Composition Comprising the Antibody of the Present Invention

The antibody of the present invention can be used as a composition forpreventing/treating cancer. The composition for preventing/treatingcancer, which comprises the antibody of the present invention, arelow-toxic and can be administered as they are in the form of liquidpreparations, or as pharmaceutical compositions of suitable preparationsto human or mammals (e.g., rats, rabbits, sheep, swine, bovine, feline,canine, simian, etc.) orally or parenterally (e.g., intravascularly,intraperitoneally, subcutaneously, etc.).The antibody of the presentinvention may be administered in itself, or may be administered as anappropriate composition. The composition used for the administration maycontain a pharmacologically acceptable carrier with the antibody of thepresent invention or its salt, a diluent or excipient. Such acomposition is provided in the form of pharmaceutical preparationssuitable for oral or parenteral administration.

Examples of the composition for parenteral administration are injectablepreparations, suppositories, etc. The injectable preparations mayinclude dosage forms such as intravenous, subcutaneous, intracutaneousand intramuscular injections, drip infusions, intraarticular injections,etc. These injectable preparations may be prepared by methods publiclyknown. For example, the injectable preparations may be prepared bydissolving, suspending or emulsifying the antibody of the presentinvention or its salt in a sterile aqueous medium or an oily mediumconventionally used for injections. As the aqueous medium forinjections, there are, for example, physiological saline, an isotonicsolution containing glucose and other auxiliary agents, etc., which maybe used in combination with an appropriate solubilizing agent such as analcohol (e.g., ethanol), a polyalcohol (e.g., propylene glycol,polyethylene glycol), a nonionic surfactant (e.g., polysorbate 80,HCO-50 (polyoxyethylene (50 mols) adduct of hydrogenated castor oil)),etc. As the oily medium, there are employed, e.g., sesame oil, soybeanoil, etc., which may be used in combination with a solubilizing agentsuch as benzyl benzoate, benzyl alcohol, etc. The injection thusprepared is usually filled in an appropriate ampoule. The suppositoryused for rectal administration may be prepared by blending the antibodyof the present invention or its salt with conventional bases forsuppositories. The composition for oral administration includes solid orliquid preparations, specifically, tablets (including dragees andfilm-coated tablets), pills, granules, powdery preparations, capsules(including soft capsules), syrup, emulsions, suspensions, etc. Such acomposition is manufactured by publicly known methods and may contain avehicle, a diluent or excipient conventionally used in the field ofpharmaceutical preparations. Examples of the vehicle or excipient fortablets are lactose, starch, sucrose, magnesium stearate, etc.

Advantageously, the compositions for oral or parenteral use describedabove are prepared into pharmaceutical preparations with a unit dosesuited to fit a dose of the active ingredients. Such unit dosepreparations include, for example, tablets, pills, capsules, injections(ampoules), suppositories, etc. The amount of the aforesaid compoundcontained is generally 5 to 500 mg per dosage unit form; it is preferredthat the antibody described above is contained in about 5 to about 100mg especially in the form of injection, and in 10 to 250 mg for theother forms.

The dose of the aforesaid prophylactic/therapeutic agent or regulatorcomprising the antibody of the present invention may vary depending uponsubject to be administered, target disease, conditions, route ofadministration, etc. For example, when used for the purpose oftreating/preventing, e.g., breast cancer in an adult, it is advantageousto administer the antibody of the present invention intravenously in adose of about 0.01 to about 20 mg/kg body weight, preferably about 0.1to about 10 mg/kg body weight and more preferably about 0.1 to about 5mg/kg body weight, about 1 to 5 times/day, preferably about 1 to 3times/day. In other parenteral and oral administration, the agent can beadministered in a dose corresponding to the dose given above. When thecondition is especially severe, the dose may be increased according tothe condition.

The antibody of the present invention may be administered as it standsor in the form of an appropriate composition. The composition used forthe administration may contain a pharmacologically acceptable carrierwith the aforesaid antibody or its salts, a diluent or excipient. Such acomposition is provided in the form of pharmaceutical preparationssuitable for oral or parenteral administration (e.g., intravascularinjection, subcutaneous injection, etc.). Each composition describedabove may further contain other active ingredients. Furthermore, theantibody of the present invention may be used in combination with otherdrugs, for example, alkylating agents (e.g., cyclophosphamide,ifosfamide, etc.), metabolic antagonists (e.g., methotrexate,5-fluorouracil, etc.), anti-tumor antibiotics (e.g., mitomycin,adriamycin, etc.), plant-derived anti-tumor agents (e.g., vincristine,vindesine, Taxol®, etc.), cisplatin, carboplatin, etoposide, irinotecan,etc. The antibody of the present invention and the drugs described abovemay be administered simultaneously or at staggered times to the patient.

The method of treatment described herein, particularly for cancers, mayalso be carried out with administration of other antibodies orchemotherapeutic agents. For example, an antibody against EGFR, such asERBITUX® (cetuximab), may also be administered, particularly whentreating colon cancer. ERBITUX® has also been shown to be effective fortreatment of psoriasis. Other antibodies for combination use includeHerceptin® (trastuzumab) particularly when treating breast cancer,AVASTIN® particularly when treating colon cancer and SGN-15 particularlywhen treating non-small cell lung cancer. The administration of theantibody of the present invention with other antibodies/chemotherapeuticagents may occur simultaneously, or separately, via the same ordifferent route.

The chemotherapeutic agent/other antibody regimens utilized include anyregimen believed to be optimally suitable for the treatment of thepatient's condition. Different malignancies can require use of specificanti-tumor antibodies and specific chemotherapeutic agents, which willbe determined on a patient to patient basis. In a preferred embodimentof the invention, chemotherapy is administered concurrently with or,more preferably, subsequent to antibody therapy. It should beemphasized, however, that the present invention is not limited to anyparticular method or route of administration.

The preponderance of evidence shows that AR53A10.11 mediates anti-cancereffects through ligation of an epitope present on cancer cell lines andhuman tumor tissue. Further it could be shown that the AR53A10.11antibody could be used in detection of cells and/or tissues whichexpress the epitope which specifically binds thereto, utilizingtechniques illustrated by, but not limited to FACS, cell ELISA or IHC.

All patents and publications mentioned in this specification areindicative of the levels of those skilled in the art to which theinvention pertains. All patents and publications are herein incorporatedby reference to the same extent as if each individual publication wasspecifically and individually indicated to be incorporated by reference.

It is to be understood that while a certain form of the invention isillustrated, it is not to be limited to the specific form or arrangementof parts herein described and shown. It will be apparent to thoseskilled in the art that various changes may be made without departingfrom the scope of the invention and the invention is not to beconsidered limited to what is shown and described in the specification.One skilled in the art will readily appreciate that the presentinvention is well adapted to carry out the objects and obtain the endsand advantages mentioned, as well as those inherent therein. Anyoligonucleotides, peptides, polypeptides, biologically relatedcompounds, methods, procedures and techniques described herein arepresently representative of the preferred embodiments, are intended tobe exemplary and are not intended as limitations on the scope. Changestherein and other uses will occur to those skilled in the art which areencompassed within the spirit of the invention and are defined by thescope of the appended claims. Although the invention has been describedin connection with specific preferred embodiments, it should beunderstood that the invention as claimed should not be unduly limited tosuch specific embodiments. Indeed, various modifications of thedescribed modes for carrying out the invention which are obvious tothose skilled in the art are intended to be within the scope of thefollowing claims.

1. An isolated monoclonal antibody produced by the hybridoma depositedwith the IDAC as accession number 141205-04 or an antigen bindingfragment thereof.
 2. A humanized antibody or an antigen binding fragmentthereof, wherein said humanized antibody binds to the antigen to whichthe monoclonal antibody of claim 1 binds and wherein said humanizedantibody comprises each of the three complementarity determining regionsof both the heavy and light chain variable domains of the monoclonalantibody.
 3. A chimeric antibody or an antigen binding fragment thereof,wherein said chimeric antibody binds to the antigen to which themonoclonal antibody of claim 1 binds and wherein said chimeric antibodycomprises the heavy and light chain variable domains of the monoclonalantibody.
 4. A conjugate of the antibody or antigen binding fragmentthereof of any one of claims 1, 2, and 3 and a member selected from thegroup consisting of a cytotoxic moiety, an enzyme, a radioactivecompound, a cytokine, an interferon, a target moiety and a reportermoiety.
 5. The isolated hybridoma cell line deposited with the IDAC asaccession number 141205-04.
 6. A composition comprising the antibody orantigen binding fragment thereof of any one of claims 1, 2, and 3, and apharmacologically acceptable carrier.
 7. A composition comprising theconjugate of claim 4; and a pharmacologically acceptable carrier.
 8. Akit comprising the isolated monoclonal antibody produced by thehybridoma deposited with the IDAC as accession number 141205-04.